Certain phosphonic acid quinoline-2-carboxylic acids, esters or amides useful for treatment of disorders responsive to N-methyl D-aspartate receptor blockade

ABSTRACT

The present invention is concerned with the phosphonic acids of formula I ##STR1## wherein one or both of the acidic hydroxy groups of the phosphonic acid moiety may be functionalized in form of pharmaceutically acceptable mono- or di- esters; wherein Y represents optionally substituted 2-carboxytetrahydroquinolinyl or 2-carboxyperhydroquinolinyl, and in each of which the carboxy group may be functionalized in form of a pharmaceutically acceptable ester or amide; A represents a direct bond, lower alkenylene, lower alkylidene or lower alkylene; and pharmaceutically acceptable salts thereof; which are useful for the treatment of nervous system disorders in mammals and as antagonists of the N-methyl-D-aspartate sensitive excitatory amino acid receptor.

This is a divisional of Ser. No. 441,497 filed Nov. 27, 1989, now U.S.Pat. No. 5,057,506, which is a divisional of Ser. No. 124,226 filed Nov.23, 1987, now U.S. Pat. No. 4,906,621, which is a continuation-in-partof Ser. No. 933,702 filed Nov. 21, 1986, now abandoned, which is acontinuation-in-part of Ser. No. 867,114 filed May 27, 1986, nowabandoned, which is a continuation-in-part of Ser. No. 738,102 filed May24, 1985, now abandoned.

SUMMARY OF THE INVENTION

The present invention is concerned with the phosphonic acids of formulaI ##STR2## wherein one or both of the acidic hydroxy groups of thephosphonic acid moiety may be functionalized in form of pharmaceuticallyacceptable mono- or di- esters; wherein Y represents optionallysubstituted 2-carboxypyrrolidinyl, 2-carboxy-2,5-dihydropyrrolyl,2-carboxy-1,2,3,6-tetrahydropyridinyl,2-carboxy-1,2,5,6-tetrahydropyridinyl, 2-carboxypiperidinyl,2-carboxytetrahydroquinolinyl, 2-carboxyperhydroquinolinyl,2-carboxy-2,3-dihydroindolyl or 2-carboxy-perhydroindolyl as describedherein, and in each of which the carboxy group may be functionalized inform of a pharmaceutically acceptable ester or amide; A represents adirect bond, lower alkenylene, lower alkylidene or lower alkyleneprovided that A does not represent a direct bond when Y represents2-carboxypyrrolidinyl; and pharmaceutically acceptable salts thereof;which are useful in mammals as antagonists of the N-methyl-D-aspartatesensitive excitatory amino acid receptor.

The instant invention is further concerned with process for preparingsaid compounds, with pharmaceutical compositions comprising saidcompounds, with a method of blocking the N-methyl-D-aspartate excitatoryamino acid receptor, and with a method of treating conditions anddiseases in mammals responsive to the effect of an excitatory amino acidreceptor antagonist by administration of said compounds or ofpharmaceutical compositions comprising said compounds.

The compounds of the invention are active and useful as selectiveantagonists of the N-methyl-D-aspartate (NMDA) excitatory amino acidreceptor. The compounds of the invention are therefore also useful,administered alone or in combination to mammals, for the treatment ofdisorders responsive to said blockade of the NMDA receptor, comprisinge.g. cerebral ischemia, muscular spasms (spasticity), convulsivedisorders (epilepsy) and anxiety. The compounds of the invention arealso contemplated to be useful for the treatment of Huntington'sdisease.

DETAILED DESCRIPTION OF THE INVENTION

One aspect of the invention relates to the phosphonic acid derivativesof formula I and derivatives thereof wherein Y represents optionallysubstituted 2-carboxypiperidinyl, 2-carboxy-1,2,3,6-tetrahydropyridinylor 2-carboxy-1,2,5,6-tetrahydropyridinyl, more specifically thecompounds of the formula II ##STR3## and the compounds of formula IIwith a double bond present between the 3 and 4 or between the 4 and 5carbon atoms of the piperidyl ring, in which the phosphono bearing chainis attached at the 3, 4, or 5- position of the piperidinyl ortetrahydropyridinyl ring, and wherein R and R' represent hydrogen, loweralkyl, benzyl, benzyl substituted on phenyl by halogen, lower alkyl orlower alkoxy, lower alkanoyloxymethyl, lower alkanoyloxymethylsubstituted on oxymethyl by lower alkyl, cyclohexyl or cyclopentyl; R₂represents hydrogen, lower alkyl, aryl-lower alkyl, or acyl; R₃represents hydrogen, lower alkyl or aryl-lower alkyl; COR₁ representscarboxy or carboxy derivatized in the form of a pharmaceuticallyacceptable ester or amide; A represents a direct bond, lower alkenylene,or lower alkylene; and pharmaceutically acceptable salts thereof.

Preferred are the said compounds, and more particularly those of formulaII, wherein R and R' independently represent hydrogen, benzyl, loweralkyl, lower alkanoyloxymethyl or lower alkanoyloxymethyl substituted onoxymethyl by lower alkyl, cyclohexyl or cyclopentyl; A represents adirect bond or alkylene of 1 to 4 carbon atoms; COR₁ represents carboxy,carbamoyl or carboxy esterified in form of a pharmaceutically acceptableester; R₂ and R₃ represent hydrogen or lower alkyl; and pharmaceuticallyacceptable salts thereof.

Also preferred are compounds of formula II wherein A representsalkenylene of 2 to 4 carbon atoms; and R, R', COR₁, R₂ and R₃ havemeaning as defined above.

Further preferred are the compounds of formula II wherein R and R'represent hydrogen, lower alkanoyloxymethyl or lower alkanoyloxymethylsubstituted on oxymethyl by lower alkyl; A is at the 4- position andrepresents a direct bond or alkylene of 1 to 4 carbon atoms; R₂ and R₃represent hydrogen; COR₁ represents carboxy, carbamoyl or carboxyesterified in form of a pharmaceutically acceptable ester; andpharmaceutically acceptable salts thereof.

Also further preferred are compounds of formula II wherein A representsalkenylene of 3 or 4 carbon atoms with double bond adjacent to phosphonogrouping, and R, R', COR₁, R₂ and R₃ have meaning as defined above.

Particularly preferred are the compounds of formula III ##STR4## whereinn represents the integer 1, 2, or 3; R and R' independently representhydrogen, lower alkyl, benzyl, lower alkanoyloxymethyl or loweralkanoyloxymethyl substituted on oxymethyl by lower alkyl; COR₁represents carboxy, carboxy esterified in the form of a pharmaceuticallyacceptable ester, or carbamoyl; R₂ represents hydrogen, lower alkyl,lower alkanoyl, benzoyl or benzoyl substituted by lower alkyl, by loweralkoxy, by halogen or by trifluoromethyl; and pharmaceuticallyacceptable salts of said compounds having a salt-forming functionalgrouping.

Most preferred are the compounds of formula III wherein the 2- and 4-substituents are cis to each other.

Further preferred are the said compounds of formula III wherein nrepresents the integer 1, 2 or 3; R and R' both represent hydrogen orlower alkanoyloxymethyl; or one of R and R' represents hydrogen and theother of R and R' represents lower alkyl, benzyl, loweralkanoyloxymethyl or lower alkanoyloxymethyl substituted on oxymethyl bylower alkyl; R₂ represents hydrogen; COR₁ represents carboxy or carboxyesterified in form of a pharmaceutically acceptable ester; andpharmaceutically acceptable salts thereof.

A preferred embodiment relates to the compounds, preferably cis, offormula III wherein n represents the integer 1, 2 or 3; R and R'represent hydrogen; COR₁ represents carboxy or carboxy esterified inform of a pharmaceutically acceptable ester; R₂ represents hydrogen; andpharmaceutically acceptable salts thereof.

A further preferred embodiment relates to the compounds of formula II,preferably cis, in which R, R', R₂ and R₃ represent hydrogen; A is atthe 4-position and represents 1,3-propenylene, preferably with doublebond adjacent to the phosphono grouping; COR₁ represents carboxy orcarboxy esterified in form of a pharmaceutically acceptable ester; andpharmaceutically acceptable salts thereof. A further particularembodiment relates to said compounds of formula II wherein A represents1,3-propenylene with double bond adjacent to the piperidine ring.

Another aspect of the invention relates to the phosphonic acidderivatives of formula I and derivatives cited above wherein Yrepresents 2-carboxy-1,2,3,4-tetrahydro- or perhydroquinolinyl in whichthe phosphono bearing chain is preferably located at the 3 or 4 positionof the tetrahydro or perhydroquinolinyl ring, i.e. the compounds offormula IV ##STR5## or perhydro derivatives thereof, wherein Arepresents lower alkylene, lower alkenylene or a direct bond; R and R'represent hydrogen, lower alkyl, benzyl, benzyl substituted on phenyl byhalogen, lower alkyl or lower alkoxy; or R and R' represent loweralkanoyloxymethyl, lower alkanoyloxymethyl substituted on oxymethyl bylower alkyl, cyclohexyl or cyclopentyl; COR₁ represents carboxy orcarboxy functionalized in the form of a pharmaceutically acceptableester or amide; R₂ represents hydrogen, lower alkyl, aryl-lower alkyl,or acyl; R₄ represents hydrogen, lower alkyl, lower alkoxy, halogen ortrifluoromethyl; and pharmaceutically acceptable salts thereof.

Preferred are the compounds of formula V ##STR6## or theperhydroquinoline derivatives thereof wherein n represents the integer1, 2, or 3; R and R' independently represent hydrogen, lower alkyl,benzyl, lower alkanoyloxymethyl or lower alkanoyloxymethyl substitutedon oxymethyl by lower alkyl; COR₁ represents carboxy, carboxy esterifiedin the form of a pharmaceutically acceptable ester, or carbamoyl; R₂represents hydrogen, lower alkyl, lower alkanoyl, benzoyl or benzoylsubstituted by lower alkyl, by lower alkoxy, by halogen or bytrifluoromethyl; and pharmaceutically acceptable salts of said compoundshaving a salt-forming functional grouping.

Most preferred are the compounds of formula V wherein the 2- and 4-substituents are cis to each other.

Further preferred are said compounds of formula V and perhydroquinolinederivatives thereof wherein n represents the integer 1, 2 or 3; R and R'both represent hydrogen or lower alkanoyloxymethyl; or one of R and R'represents hydrogen and the other of R and R' represents lower alkyl,benzyl, lower alkanoyloxymethyl, or lower alkanoyloxymethyl substitutedon oxymethyl by lower alkyl; R₂ represents hydrogen; COR₁ representscarboxy or carboxy esterified in form of a pharmaceutically acceptableester; and pharmaceutically acceptable salts thereof.

A preferred embodiment relates to the compounds, preferably cis, offormula V and the perhydroquinoline derivatives thereof wherein nrepresents the integer 1; R and R' represent hydrogen; COR₁ representscarboxy or carboxy esterified in form of a pharmaceutically acceptableester; R₂ represents hydrogen; and pharmaceutically acceptable saltsthereof.

Another preferred embodiment relates to the compounds of formula IV andthe perhydroquinoline derivatives thereof wherein A is attached at the 4position and represents 1,3-propenylene with double bond adjacent to thephosphono grouping; R, R' and R₂ and R₄ represent hydrogen; COR₁represents carboxy or carboxy esterified in form of a pharmaceuticallyacceptable ester; and pharmaceutically acceptable salts thereof.

A further aspect of the invention relates to the phosphonic acidderivatives of formula I and derivatives cited above wherein Yrepresents optionally substituted 2-carboxypyrrolidinyl, i.e. thecompounds of formula VI ##STR7## and the compounds of formula VI with adouble bond present between the 3 and 4 carbon atoms of the pyrrolidinylring, in which the phosphono bearing chain is attached preferably at the3 or 4 position of the pyrrolidine ring and wherein R and R' representhydrogen, lower alkyl, benzyl, benzyl substituted on phenyl by halogen,lower alkyl, or lower alkoxy, or R and R' represent loweralkanoyloxymethyl, lower alkanoyloxymethyl substituted on oxymethyl bylower alkyl, cyclohexyl or cyclopentyl; R₂ represents hydrogen, loweralkyl, or acyl; R₃ represents hydrogen, lower alkyl or aryl-lower alkyl;COR₁ represents carboxy or carboxy derivatized in the form ofpharmaceutically acceptable ester or amide; A represents lower alkyleneor lower alkenylene; and pharmaceutically acceptable salts thereof.

Preferred are the compounds of formula VI wherein the phosphono bearinggroup is attached at the 3 or 4-position; R₂ and R₃ represent hydrogen;R and R' represent hydrogen or lower alkanoyloxymethyl; COR₁ representscarboxy, carbamoyl or carboxy esterified in form of a pharmaceuticallyacceptable ester; A represents methylene, ethylene, or propylene; andpharmaceutically acceptable salts.

Further preferred are the compounds of formula VI wherein the phosphonobearing group is attached at the 3-position; R₂ and R₃ representhydrogen; R and R' represent hydrogen; COR₁ represents carboxy orcarboxy esterified in the form of a pharmaceutically acceptable ester; Arepresents methylene, ethylene or propylene; and pharmaceuticallyacceptable salts.

Also further preferred are the compounds of formula VI wherein thephosphono bearing group A is attached at the 3-position; R, R', R₂, R₃and COR₁ have meaning as defined above; and A represents 1,3-propenylenewith double bond adjacent to the phosphono grouping; andpharmaceutically acceptable salts thereof.

The general definitions used herein have the following meaning in thecontext of the invention.

The term "lower", when referred to above and hereinafter in connectionwith organic groups, radicals or compounds respectively, defines suchwith up to and including 7, preferably up to and including 4 andadvantageously one, two or three carbon atoms.

A lower alkyl group preferably contains 1-4 carbon atoms and representsfor example ethyl, propyl, butyl and advantageously methyl.

A lower alkylene linking group preferably contains 1-4 carbon atoms andrepresents for example methylene, ethylene, propylene, i.e. 1,2- or1,3-propylene, butylene, i.e. 1,2-, 1,3- or 1,4-butylene.

A lower alkenylene linking group representing A or A' preferablycontains 2 to 4 carbon atoms and represents for example ethenylene,1,3-propenylene, 1,4-but-1-enylene, 1,4-but-2-enylene, advantageouslywith double bond adjacent to phosphono grouping.

A lower alkylidene linking group representing A or A' preferablycontains 1 to 4 carbon atoms and represents for example methylidene,ethylidene, or straight chain propylidene, the double bond beingexocyclic to the ring in Y.

A lower alkoxy group preferably contains 1-4 carbon atoms and representsfor example, ethoxy, propoxy or advantageously methoxy.

Lower alkanoyl preferably contains 2-7 carbon atoms and representsadvantageously acetyl, propionyl, n-butyryl, isobutyryl or pivaloyl.

Lower alkanoyloxy represents advantageously acetoxy, propionyloxy, n- ori- butyryloxy or pivaloyloxy (trimethylacetyloxy).

Halogen is preferably fluorine and chlorine, but may also representbromine or iodine.

Aroyl represents arylcarbonyl, preferably benzoyl or benzoyl substitutedby one to three substituents selected from lower alkyl, lower alkoxy,trifluoromethyl and halogen; or pyridylcarbonyl, particularlynicotinoyl.

Aroyloxy represents preferably benzoyloxy, benzoyloxy substituted on thephenyl ring by lower alkyl, halogen or lower alkoxy, e.g. methyl, chloroor methoxy respectively; or nicotinoyloxy.

Aryl represents preferably optionally substituted phenyl, e.g. phenyl orphenyl substituted by one to three substituents selected from loweralkyl, lower alkoxy, trifluoromethyl and halogen; or pyridyl,particularly 3-pyridyl.

Aryl-lower alkyl represents preferably aryl-C₁ -C₄ -alkyl, aryl havingmeaning as defined above, advantageously benzyl or 2-phenylethyl.

Acyl represents carboxy derived acyl, preferably lower alkanoyl,aryl-lower alkanoyl, aroyl, lower alkoxycarbonyl, aryl-loweralkoxycarbonyl, alpha-amino-lower alkanoyl or alpha-amino-aryl-loweralkanoyl.

Aryl-lower alkanoyl represents preferably aryl-C₁ -C₄ -alkanoyl,advantageously phenylacetyl or 3-phenylpropionyl.

A lower alkoxycarbonyl group preferably contains 1-4 carbon atoms in thealkoxy portion and represents for example: methoxycarbonyl,propoxycarbonyl, isopropoxycarbonyl or advantageously ethoxycarbonyl. AnN-mono(lower alkyl)-carbamoyl group preferably contains 1-4 carbon atomsin the alkyl portion and is for example N-methylcarbamoyl,N-propylcarbamoyl, or advantageously N-ethylcarbamoyl.

Aryl-lower alkoxycarbonyl represents preferably benzyloxycarbonyl.

Alpha-amino-lower alkanoyl and alpha-amino-aryl-lower alkanoylrepresents acyl groups of alpha-aminoacids, such as alanyl, glycyl,leucyl, isoleucyl, phenylalanyl and the like.

An N,N-di(lower alkyl)-carbamoyl group preferably contains 1-4 carbonatoms in each lower alkyl portion and represents for exampleN,N-dimethylcarbamoyl, N-methyl-N-ethylcarbamoyl and advantageouslyN,N-diethylcarbamoyl.

A di-lower alkylamino-N-lower alkylcarbamoyl group preferably representsdi-C₁ -C₄ -alkylamino-N-C₂ -C₄ -alkylcarbamoyl, the two nitrogen atomsbeing separated by 2-4 carbon atoms and represents for exampleN-(2-diethylaminoethyl)carbamoyl, N-(3-diethylaminopropyl)carbamoyl.

A mono-lower alkylamino group preferably contains 1-4 carbon atoms andrepresents for example methylamino, ethylamino, n or i-(propylamino orbutylamino).

A di-lower alkylamino group preferably contains 1-4 carbon atoms in eachlower alkyl group and represents for example dimethylamino,diethylamino, di-(n-propyl)-amino and di-(n-butyl)-amino).

A di-lower alkylamino - lower alkoxycarbonyl group contains preferably2-4 carbon atoms in the alkoxy portion, the oxygen and nitrogen atomsbeing separated by 2-4 carbon atoms, and for example representsN,N-diethylaminoethoxycarbonyl or N,N-diethylamino-propoxycarbonyl.

A pharmaceutically acceptable ester within the context of the presentinvention represents an ester of a compound of the invention having acarboxy group, preferably a carboxylic acid prodrug ester that may beconvertible under physiological conditions to the corresponding freecarboxylic acid.

Carboxy esterified in form of a pharmaceutically acceptable ester,preferably represents e.g. lower alkoxycarbonyl; (amino, mono- ordi-lower alkylamino)-substituted straight chain C₂ -C₅ loweralkoxycarbonyl; carboxy substituted lower alkoxycarbonyl, e.g.α-carboxy-substituted lower alkoxycarbonyl; loweralkoxycarbonyl-substituted lower alkoxycarbonyl, e.g. α-loweralkoxycarbonyl-substituted lower alkoxycarbonyl; aryl-substituted loweralkoxycarbonyl, e.g. unsubstituted or substituted benzyloxycarbonyl orpyridylmethoxycarbonyl; lower alkanoyloxy-substituted methoxycarbonyl,e.g. pivaloyloxymethoxycarbonyl; (lower alkanoyloxy or loweralkoxy)-substituted lower alkoxymethoxy carbonyl;bicyclo[2,2,1]heptyloxycarbonyl-substituted methoxycarbonyl such asbornyloxycarbonylmethoxycarbonyl; 3-phthalidoxycarbonyl; (lower alkyl,lower alkoxy, halo)substituted 3-phthalidoxycarbonyl; loweralkoxycarbonyloxylower alkoxycarbonyl, e.g. 1-(methoxy- orethoxycarbonyloxy)-ethoxycarbonyl.

Most preferred prodrug esters are e.g. the straight chain C₁ -C₄ -alkylesters such as ethyl; the lower alkanoyloxymethyl esters such aspivaloyloxymethyl; the di-lower alkylamino-straight chain C₂ -C₄ -alkylesters such as 2-diethyl-aminoethyl; the pyridylmethyl esters such as3-pyridylmethyl.

A pharmaceutically acceptable amide within the context of the presentinvention represents an amide of a compound of the invention having acarboxy group, preferably a carboxylic acid amide that may beconvertible under physiological conditions to the corresponding freecarboxylic acid.

Preferred amides are compounds of the invention wherein carboxy isderivatized as carbamoyl, N-mono-lower alkylcarbamoyl such asN-ethylcarbamoyl, N,N-di-lower alkylcarbamoyl such asN,N-diethylcarbamoyl, or di-lower aklylamino-N-lower alkylcarbamoyl suchas N-(2-diethylaminoethyl)carbamoyl orN-(3-diethylaminopropyl)carbamoyl.

Pharmaceutically acceptable salts are preferably metal or ammonium saltsor said compounds of the invention having a free phosphonic or carboxygroup, more particularly alkali or alkaline earth metal salts, e.g. thesodium, potassium, magnesium or calcium salt; or advantageouslycrystallizing ammonium salts derived from ammonia or organic amines,such as methylamine, diethylamine, triethylamine, dicylohexylamine,triethanolamine, ethylenediamine, tris-(hydroxymethyl)aminomethane orbenzyltrimethylammonium hydroxide. The compounds of the invention whichare basic amines form acid addition salts of preferably pharmaceuticallyacceptable inorganic or organic acids, such as of strong mineral acids,for example hydrohalic, e.g. hydrochloric or hydrobromic acid; sulfuric,phosphoric or nitric acid; aliphatic or aromatic carboxylic or sulfonicacids, e.g. acetic, propionic, succinic, glycolic, lactic, malic,tartaric, gluconic, citric, ascorbic, maleic, fumaric, pyruvic, pamoic,nicotinic, methanesulfonic, ethanesulfonic, hydroxyethanesulfonic,benzenesulfonic, p-toluenesulfonic or naphthalenesulfonic acid.

The compounds of the invention exhibit valuable pharmacologicalproperties, e.g. by selectively blocking the N-methyl-D-aspartateexcitatory aminoacid receptors in mammals. The compounds are thus usefulfor treating diseases responsive to excitatory amino acid blockade inmammals, comprising e.g. cerebral ischemia and nervous system disorders,particularly convulsive disorders (epilepsy) and anxiety.

These effects are demonstrable in in vitro tests or in vivo animal testsusing advantageously mammals or tissues or enzyme preparations thereof,e.g. mice, rats, or monkeys. Said compounds can be administered to thementerally or parenterally, advantageously orally or transdermally, orsubcutaneously, intravenously or intraperitoneally, for example, withingelatin capsules, or in the form of aqueous suspensions or solutions,respectively. The applied in vivo dosage may range between about 0.01 to100 mg/kg, preferably between about 0.05 and 50 mg/kg, advantageouslybetween about 0.1 and 10 mg/kg. Said compounds can be applied in vitroin the form of e.g. aqueous solutions and the dosage may range betweenabout 10⁻⁴ molar and 10⁻⁸ molar concentrations.

The inhibitory effect on the NMDA-type excitatory amino acid receptorsis determined in vitro by measuring the inhibition of the NMDA-evoked ³H-acetylcholine (³ H-ACh) release from corpus striatum tissue of ratbrain, according to J. Lehmann and B. Scatton, Brain Research 252, 77-89(1982) and Nature 297, 422-424 (1982).

Antagonists of NMDA-type excitatory amino acid receptors competitivelyantagonize NMDA-evoked ³ H-acetylcholine (³ H-ACh) release from corpusstriatum tissue of the brain.

The inhibition of the NMDA-evoked ³ H-acetylcholine (³ H-ACh) releasefrom rat striatal tissue slices by a compound of the invention isexpressed as % of release of ³ H-ACh in response to stimulation with 50uM NMDA compared to control. Tests are two-tailed with a minimum of n=4in each group. In IC₅₀ values represent the concentration of testcompound required to inhibit the NMDA-increased ³ H-ACh release by 50%.

Illustrative of the invention,cis-4-phosphonomethyl-2-piperidinecarboxylic acid hydrochloride has anIC₅₀ of about 8×10⁻⁶ M in the in vitro NMDA-evoked ³ H-ACh release test.

The inhibitory effect on the NMDA-type excitatory amino acid receptorsis demonstrated in vivo by inhibition of NMDA-induced convulsions in themouse.

Illustrative of the invention,cis-4-phosphonomethyl-2-piperidinecarboxylic acid hydrochloride preventsNMDA-induced convulsions in the mouse at a dose of about 2.3 mg/kg i.p.;cis 4-[1-(3-phosphonoprop-1-enyl)]-piperidine-2-carboxylic acid issimilarly effective at a dose of about 1.2 mg/kg i.p..

Further indicative of the anticonvulsant activity, compounds of theinvention are effective in preventing audiogenic-induced seizures inDBA/2 mice (Chapman et al., Arzneim.-Forsch. 34:1261, 1984).

The effect is determined as follows:

Forty-five minutes following compound or vehicle administration, miceare placed individually in a soundproof chamber. After a 30 secondaccommodation period, the mice are exposed to a sound stimulation of 110dB for 1 minute or until the appearance of a tonic-clonic seizure.Control seizures consist of an initial wild running phase. Theprevention of wild running is indicative of an anticonvulsant effect.

Test compounds in either distilled water solution or in a 3% (w/v)colloidal cornstarch suspension containing 5% (w/v) polyethyleneglycol400 and 0.34% (w/v) Tween 80, are administered by oral intubation orintraperitoneally in a volume of 10 ml/kg of body weight.

Illustrative of the invention,cis-4-phosphonomethyl-2-piperidinecarboxylic acid hydrochloride iseffective in the audiogenic-induced seizure model in mice with an ED₅₀of about 1.8 mg/kg on i.p. administration.

Indicative of anxiolytic activity, compounds of the invention areeffective in the Cook/Davidson conflict model (Psychopharmacologia 15,159-168 (1969).

Illustrative of the invention,cis-4-phosphonomethyl-2-piperidine-carboxylic acid is active in theCook/Davidson test for anxiolytic activity at a dose of about 2 mg/Kgi.p.

The cerebral antiischemic activity, that is the effect of the compoundsof the invention in preventing or reducing brain damage in mammals dueto a transient cerebral ischemia (as in a stroke) can be determined inthe mongolian gerbil ischemia model, e.g. the model described by T.Kirino, Brain Research 239, 57-69 (1982).

The inhibitory effect on the observed hyperactivity and on thedegeneration of neurons in the hippocampus region of the brain followinga 5-minute period of ischemia is measured.

The test compound is administered i.p. 15 minutes before the ischemia or2, 4, and 6 hours post ischemia.

Illustrative of the invention,cis-4-phosphonomethyl-2-piperinecarboxylic acid, at a dose of 10 mg/Kgip administered either before or after the ischemia episode, inhibitsthe ischemia-induced hyperactivity of the gerbil and reduces thedegeneration of cerebral neurons as measured in the hippocampus regionof the brain.

The aforementioned advantageous properties render the compounds of theinvention useful as antagonists of the N-methyl-D-aspartate excitatoryamino acid receptor in mammals and for the treatment of conditionsresponsive thereto, such as cerebral ischemia, anxiety and convulsivedisorders.

The compounds of the invention, i.e. the compounds of formula I citedhereinabove, are prepared by

a) for compounds of formula I wherein A represents a direct bond orlower alkylene, reducing the pyrrolyl, pyridinyl, indolyl orquinolinylring in a compound of the formula ##STR8## or a functional phosphonicacid derivative thereof as defined above, wherein A represents a directbond or lower alkylene; and wherein Y_(a) represents an unsaturated formof Y, namely 2-carboxypyrrolyl, 2-carboxypyridinyl, 2-carboxyquinolinylor 2-carboxyindolyl all optionally substituted as defined for Y, andwherein the carboxy group may be functionalized in form of an ester oramide as defined above; or reducing a double bond in a compound of theformula ##STR9## wherein Y has meaning as defined above, or a functionalphosphonic acid derivative thereof, A' represents lower alkenylene orlower alkenylidene with the double bond attached to Y; or

b) condensing a reactive ester derivative of a compound of the formula

    Y--A--OH                                                   (VIII)

wherein Y and A have meaning as defined above with a diester ofphosphorous acid, of the formula IX or with a phosphorus trihalide or aphosphorus tri-(lower)alkoxide of formula X ##STR10## wherein R"advantageously represents lower alkyl and, if required, converting theresulting phosphonic acid derivative to the phosphonic acid or otherester derivative thereof;

c) converting to COR₁ a substituent other than COR₁ at position 2 of thepiperidinyl, tetrahydro-pyridinyl, 1,2,3,4-tetrahydroquinolinyl,perhydroquinolinyl, dihydropyrrolyl, pyrrolidinyl, 2,3-dihydroindolyl orperhydroindolyl ring in a compound otherwise identical to a compound ofthe invention; and carrying out the said processes while, if necessary,temporarily protecting any interfering reactive group(s) in theseprocesses, and then liberating the resulting compound of the invention;and, if desired, converting a resulting compound of the invention intoanother compound of the invention, and/or, if desired, converting aresulting free compound into a salt or a resulting salt into the freecompound or into another salt; and/or separating a mixture of isomers orracemates obtained into the single isomers or racemates; and/or, ifdesired, resolving a racemate obtained into the optical antipodes.

A reactive ester derivative of a compound, in any of the hereinmentioned processes, having a hydroxy group, e.g. of a compound offormula VIII, represents a compound wherein hydroxy is esterified by astrong acid, especially hydrochloric, hydrobromic or hydriodic acid, orsulphuric acid, or by a strong organic acid, especially a strong organicsulfonic acid, such as an aliphatic or aromatic sulfonic acid, forexample methanesulfonic acid, 4-methylphenylsulfonic acid or4-bromophenylsulfonic acid. Said reactive esterified hydroxy group isespecially halo, for example chloro, bromo or iodo, or aliphatically oraromatically substituted sulfonyloxy, for example methanesulfonyloxy,phenylsulfonyloxy or 4-methylphenylsulfonyloxy (tosyloxy).

In starting compounds and intermediates therefor which are converted tothe compounds of the invention in a manner described herein, functionalgroups present, such as carboxy, amino (including ring NH) and hydroxygroups, are optionally protected by conventional protecting groups thatare common in preparative organic chemistry. Protected carboxy, aminoand hydroxy groups are those that can be converted under mild conditionsinto free carboxy, amino and hydroxy groups without the molecularframework being destroyed or other undesired side reactions takingplace.

The purpose of introducing protecting groups is to protect thefunctional groups from undesired reactions with reaction components andunder the conditions used for carrying out a desired chemicaltransformation. The need and choice of protecting groups for aparticular reaction is known to those skilled in the art and depends onthe nature of the functional group to be protected (carboxy group, aminogroup, etc.), the structure and stability of the molecule of which thesubstituent is a part, and the reaction conditions.

Well-known protecting groups that meet these conditions and theirintroduction and removal are described, for example, in J. F. W. McOmie,"Protective Groups in Organic Chemistry", Plenum Press, London, New York1973, T. W. Greene, "Protective Groups in Organic Synthesis", Wiley, NewYork 1981, and also in "The Peptides", Vol. I, Schroeder and Luebke,Academic Press, London, New York 1965, as well as in Houben-Weyl,"Methoden der Organischen Chemie", Vol. 15/1, George Thieme Verlag,Stuttgart, 1974.

The preparation of the compounds of the invention according to process(a) relating to reduction of a compound of formula VII is carried out bymethods known in the art for the reduction of pyrrole, pyridine, indoleand quinoline rings. For example, the reduction of the pyridine orquinoline ring is advantageously carried out with an organometallicreducing agent or by catalytic hydrogenation e.g. in the presence ofplatinum oxide and an acidic solvent such as acetic acid to givecorresponding tetrahydropyridines, piperidines,1,2,3,4-tetrahydroquinolines or perhydroquinolines of the invention,i.e. of formula II, IV and derivatives thereof. Quarternary quinoliniumand pyridinium compounds, e.g. in which R₂ is lower alkyl or aryl-loweralkyl, may be similarly reduced.

The starting compounds of formula VII, e.g. the quinoline and pyridinederivatives for said process (a) are prepared, e.g., by first condensinga compound R₃ -substituted-(3,-4-or 5-pyridinyl)-A--OH or R₄-substituted-(3-or 4-quinolinyl)-A--OH (A, R₃ and R₄ having meaning asdefined above) in form of a reactive ester derivative, e.g. a halidesuch as a chloride or bromide, with a diester of formula IX in thepresence of a strong base, e.g. as described in Chemical Abstracts 61,10703, or with a tri-(lower)alkyl phosphite of formula X to give thecorresponding ##STR11## in which A, R", R₃ and R₄ are as definedhereinabove.

Subsequent treatment with e.g. a peracid, such as m-chloroperbenzoicacid gives the corresponding pyridine-N-oxides or quinoline-N-oxides.Condensation with a reactive cyanide, e.g. a trialkylsilyl cyanide suchas trimethylsilyl cyanide, preferably under basic conditions, e.g. inthe presence of triethylamine, gives the corresponding 2-cyanopyridineor 2-cyanoquinoline derivatives. The cyano group in the 2-cyanopyridineand 2-cyanoquinoline derivatives are then converted, by methods known inthe art, to the 2-COR₁ (carboxy, esterified carboxy or optionallysubstituted carbamoyl substituted)pyridine and quinoline derivatives asdefined hereinabove.

Intermediates of formula VII also inhibit the N-methyl-D-aspartateexcitatory aminoacid receptors in mammals. Preferred are said compoundsof formula VII wherein Ya represents 2-carboxypyridinyl optionallysubstituted as defined hereinabove.

The preparation of the compounds of formula I and derivatives (wherein Arepresents lower alkylene) according to process (a) relating to thereduction of the double bond in a compound of formula VIIa, is carriedout by e.g. catalytic hydrogenation.

Compounds of formula VIIa are equivalent to the compounds of formula Iwherein A represents lower alkenylene or lower alkylidene which, inaddition to being useful as intermediates, are also useful asantagonists of the N-methyl-D-aspartate excitatory amino acid receptoras described herein for compounds of the invention.

The compounds of formula VIIa and derivatives thereof may be prepared,e.g. by reacting an aldehyde or ketone (including oxo derivatized Y)with e.g. a tetra-lower alkyl ester of methylenediphosphonic acid underbasic conditions, thereby adding the phosphonomethylidene grouping toobtain a compound of formula VIIa (wherein the double bond is adjacentto the phosphono grouping), and by other methods illustrated herein,e.g. using processes b) and c).

The preparation of the compounds of the invention wherein A representslower alkenylene and wherein the double bond is adjacent to thephosphono grouping involving the condensation of an aldehyde or ketonewith e.g. a tetra lower alkyl ester of methylenediphosphonic acid iscarried out according to procedure known in the art for suchcondensations, in the presence of a strong anhydrous base, e.g. butyllithium, in an inert polar solvent such as tetrahydrofuran, preferablyat reflux temperature. The starting aldehydes or ketones can be preparede.g. by oxidation of the corresponding alcohols for example withpyridinium chlorochromate, or other methods as illustrated in theexamples. The aldehydes or ketones so obtained may also be converted toaldehydes or ketones of longer chain length using conventionalmethodology, e.g. by a Wittig condensation of an aldehyde withmethoxy-methyl-triphenylphosphonium chloride to yield the homologousaldehyde, and by other well-known sequences of reactions described inthe examples.

The condensation according to process (b) is advantageously used for thepreparation of the compounds of formula I wherein the double bond withinthe alkenylene grouping A is not adjacent to the phosphono grouping. Thecorresponding starting materials of formula VIII and reactivederivatives thereof can be prepared by methods well known in the art,starting from intermediates wherein A represents lower alkylene, thepreparation of which is described above. For example, the startingmaterial of formula VIII wherein A represents lower alkenylene isprepared by condensing an aldehyde with a suitable Wittig reagent, e.g.formylmethylene-triphenyl- phosphoran, reducing the resultingunsaturated aldehyde (in which the chain has been lengthened by twocarbon atoms) to the alcohol e.g. with sodium borohydride, andconverting the resulting unsaturated alcohol to a reactive derivative,e.g. to the bromide with triphenylphosphine/N-bromo-succinimide.

The condensation according to process (b) of a reactive ester derivativeof a compound of formula VIII with a compound of formula X, e.g.triethyl phosphite, is carried out, e.g. by heating in an inert solvent,and under conditions known in the art for a Michaelis-Arbuzov reactionaccording to Angew. Chem. Int. Ed. 16, 477 (1977) and Chem. Rev. 81, 415(1981). Similarly, condensation with phosphorus trichloride andsubsequent hydrolysis gives a compound of formula I.

The condensation according to process (b) of a reactive ester derivativeof a compound of formula VIII with a compound of formula IX, e.g.diethylphosphonate (diethyl phosphite), is carried out e.g. in a strongbasic medium, for instance in the presence of an alkali metal such assodium, an alkali metal hydride such as sodium hydride, an alkali metalalkoxide such as potassium t-butoxide, in an inert solvent such astoluene or dimethylformamide.

The starting materials of formula VIII are either known in the art orare prepared by methods known in the art, e.g. by reduction of thecorresponding pyridinyl, indolyl and quinolinyl compounds, or asdescribed herein.

Interconversions according to process (c) are carried out by methodswell-known in the art.

Groups convertible into a COR₁ group are, for example, carboxy groups inform of anhydrides or acid halides, cyano, amidino groups, includingcyclic amidino groups such as 5-tetrazolyl, iminoether groups, includingcyclic iminoether groups, e.g., dihydro-2-oxazolinyl ordihydro-2-oxazolinyl groups substituted by lower alkyl, and alsohydroxymethyl, etherified hydroxymethyl, lower alkanoyloxymethyl,trialkoxymethyl, acetyl, trihaloacetyl, halomethyl, carboxycarbonyl(COCOOH), formyl (CHO), di(lower)alkoxymethyl, alkylenedioxymethyl orvinyl.

Certain terms used in the processes have the meanings as defined below.

Trialkoxymethyl represents preferably tri(lower alkoxy)-methyl,particularly triethoxy- or trimethoxymethyl.

Etherified hydroxymethyl represents preferably lower alkoxymethyl, loweralkoxyalkoxymethyl such as methoxymethyloxymethyl, 2-oxa- or2-thiacyclo- alkoxymethyl, particularly 2-tetrahydropyranyloxymethyl.

Halomethyl represents especially chloromethyl but may also bebromomethyl or iodomethyl.

An alkali metal represents preferably lithium but may also be potassiumor sodium.

Groups convertible into COR₁ =carboxy include esters and amides, andsuch are not limited to ester and amide derivatives as defined hereinfor COR₁. Conversion to carboxy is generally accomplished by solvolysis,with acid or base.

Benzyl esters or nitrobenzyl esters may be converted into the carboxygroup by catalytic hydrogenation, the latter also with chemical reducingagents, e.g., sodium dithionite or with zinc and a carboxylic acid. Inaddition, tert-butyl esters may also be cleaved with trifluoroaceticacid.

Acetyl may be oxidatively cleaved to carboxy by conversion first totrihaloacetyl, e.g. tribromo or triiodoacetyl, by treatment e.g. withsodium hypobromite, followed by cleavage with e.g. an aqueous base, suchas sodium hydroxide.

Formyl, di(lower)-alkoxymethyl or alkylenedioxymethyl (formyl protectedin the form of an acetal), e.g. the dimethyl acetal, are oxidized withe.g. silver nitrate, pyridinium dichromate or ozone to carboxy.

Vinyl may be converted to carboxy by ozonolysis to formyl, which is inturn oxidized to carboxy.

Hydrolysis of trialkoxymethyl to carboxy is advantageously carried outwith inorganic acids such as hydrohalic or sulfuric acid. Hydrolysis ofetherified hydroxymethyl to hydroxymethyl is preferably carried out withsolutions of inorganic acids such as a hydrohalic acid. Hydroxymethyl isin turn oxidized to carboxy with an oxidizing agent such as pyridiniumdichromate.

Halomethyl may also be converted to the corresponding carboxaldehydeswith e.g. dimethylsulfoxide in the presence of triethylamine and silvertetrafluoroborate, or with chromium trioxide and pyridine in methylenechloride.

The conversion of cyano to lower alkoxycarbonyl is advantageouslycarried out by treatment first with a lower alkanol, e.g. anhydrousethanol, in the presence of a strong acid, e.g. hydrochloric acidpreferably at reflux temperature, followed by hydrolysis with water.

Furthermore, the conversion of cyano to carbamoyl is preferably carriedout by treatment with an alkali metal hydroxide, e.g. dilute sodiumhydroxide, and hydrogen peroxide, preferably at room temperature.

Esterified carboxy such as lower alkoxycarbonyl may be amidized withammonia, mono- or di-(lower)alkylamines e.g. methylamine, dimethylaminein an inert solvent, e.g. a lower alkanol, such as butanol, tounsubstituted, mono- or di(lower) alkylcarbamoyl.

The compounds of the invention may thus also be converted to othercompounds of the invention by e.g. functional group transformationswell-known in the art.

For example, conversion of carboxylic acid esters and amides tocarboxylic acids is advantageously carried out by hydrolysis withinorganic acids such as a hydrohalic or sulfuric acid or with aqueousalkalies, preferably alkali metal hydroxides such as lithium or sodiumhydroxide.

Free carboxylic acids may be esterified with lower alkanols, such asethanol, in the presence of a strong acid, e.g. sulfuric acid, or withdiazo (lower) alkanes, e.g. diazomethane in a solvent such as ethylether, advantageously at room temperature, to give the correspondinglower alkyl esters.

Furthermore, the free carboxylic acids may be converted via treatment ofa reactive intermediate thereof, e.g. an acyl halide such as the acidchloride, or a mixed anhydride, e.g. such derived from a lower alkylhalocarbonate such as ethyl chloroformate, with ammonia, mono- ordi-(lower) alkylamines, in an inert solvent such as methylene chloride,preferably in the presence of a basic catalyst such as pyridine, tocompounds wherein COR₁ represents unsubstituted, mono or di-(lower)-alkylcarbamoyl.

Phosphonic acid esters are converted to the corresponding phosphonicacids by treatment with acid, such as aqueous hydrochloric acid orhydrobromic acid in glacial acetic acid, or with bromotrimethylsilaneaccording to J. Chem. Soc. Chem. Comm. 1979, 739. Benzyl esters may beconverted to the acids by hydrogenolysis.

Phosphonic acids are converted to esters, e.g. optionally substitutedlower alkyl esters, e.g. by condensation with an optionally substitutedlower alkyl halide preferably in a basic non-aqueous medium, such as inthe presence of triethylamine.

The compounds of the invention wherein Y represents optionallysubstituted 2-carboxy-(tetrahydropyridinyl, tetrahydroquinolinyl,dihydroindolyl or dihydropyrrolyl) and derivatives thereof are convertedto the corresponding piperidinyl, perhydroquinolinyl, perhydroindolyl orpyrrolidinyl compounds, respectively, e.g. by catalytic hydrogenation.

The above-mentioned reactions are carried out according to standardmethods, in the presence or absence of diluents, preferably such as areinert to the reagents and are solvents thereof, of catalysts, condensingor said other agents respectively and/or inert atmospheres, at lowtemperatures, room temperature or elevated temperatures preferably atthe boiling point of the solvents used, and at atmospheric orsuper-atmospheric pressure. The preferred solvents, catalysts andreaction conditions are set forth in the appended illustrative examples.

The invention further includes any variant of the present processes, inwhich an intermediate product obtainable at any stage thereof is used asstarting material and the remaining steps are carried out, or theprocess is discontinued at any stage thereof, or in which the startingmaterials are formed under the reaction conditions, or in which thereaction components are used in the form of their salts or opticallypure antipodes.

Mainly those starting materials should be used in said reactions, thatlead to the formation of those compounds indicated above as beingespecially preferred.

The invention also relates to any novel starting materials and processesfor their manufacture.

Depending on the choice of starting materials and methods, the newcompounds may be in the form of one of the possible isomers or mixturesthereof, for example, depending on the number of asymmetrical carbonatoms, as pure optical isomers, such as antipodes, or as mixtures ofoptical isomers such as racemates or as mixtures of diastereoisomers orof geometric isomers. The aforesaid possible isomers or mixtures thereofare within the purview of this invention; certain particular isomers arepreferred as indicated above.

Any resulting mixtures of diastereoisomers, mixtures of racemates can beseparated on the basis of the physicochemical differences of theconstituents, in known manner, into the pure isomers, diastereoisomers,racemates, or geometric isomers, for example by chromatography and/orfractional cyrstallization.

Any resulting racemates can be resolved into the optical antipodes byknown methods, for example by e.g. reacting an acidic end product withan optically active base that forms salts with the racemic acid, andseparating the salts obtained in this manner, for example by fractionalcrystallization, into the diastereoisomeric salts from which theoptically active free carboxylic or phosphonic acid antipodes can beliberated on acidification. The basic racemic products can likewise beresolved into the optical antipodes, e.g. by separation of thediastereoisomeric salts thereof, with an optically active acid, andliberating the optically active basic compound by treatment with astandard base. Racemic products of the invention can thus be resolvedinto their optical antipodes, e.g., by the fractional crystallization ofd- or 1-(tartrates, mandelates, camphorsulfonates) or of d- or1-(α-methylbenzylamine, cinchonidine, cinchonine, quinine, quinidine,ephedrine, dehydroabietylamine, brucine or strychnine) salts. The acidiccompounds of the invention can also be resolved by separatingdiastereomeric ester or amide derivatives prepared from an opticallyactive alcohol or amine, and regenerating the reduced optically activecompound. Advantageously, the more active of the two antipodes isisolated.

Finally the compounds of the invention are either obtained in the freeform, or as a salt thereof. Any resulting base can be converted into acorresponding acid addition salt, preferably with the use of atherapeutically useful acid or anion exchange preparation, or resultingsalts can be converted into the corresponding free bases, for example,with the use of a stronger base, such as a metal or ammonium hydroxideor a basic salt, e.g. an alkali metal hydroxide or carbonate, or acation exchange preparation, or an alkylene oxide such as propyleneoxide. A compound of the invention with a free carboxylic or phosphonicacid group can thus also be converted into the corresponding metal orammonium salts. These or other salts, for example, the picrates, canalso be used for purification of the bases obtained; the bases areconverted into salts, the salts are separated and the bases areliberated from the salts.

In view of the close relationship between the free compounds and thecompounds in the form of their salts, whenever a compound is referred toin this context, a corresponding salt is also intended, provided such ispossible or appropriate under the circumstances.

The compounds, including their salts, can also be obtained in the formof their hydrates, or include other solvents used for theircrystallization.

The pharmaceutical compositions according to the invention are thosesuitable for enteral, such as oral or rectal, transdermal and parenteraladministration to mammals, including man, for blockade of theN-methyl-D-aspartate excitatory amino acid receptor and for thetreatment of diseases responsive to blockade of the N-methyl-D-aspartateexcitatory amino acid receptor, such as cerebral ischemia, convulsivedisorders and anxiety, comprising an effective amount of apharmacologically active compound of the invention, alone or incombination with one or more pharmaceutically acceptable carriers.

The pharmacologically active compounds of the invention are useful inthe manufacture of pharmaceutical compositions comprising an effectiveamount thereof in conjunction or admixture with excipients or carrierssuitable for either enteral or parenteral application. Preferred aretablets and gelatin capsules comprising the active ingredient togetherwith a) diluents, e.g. lactose, dextrose, sucrose, mannitol, sorbitol,cellulose and/or glycine; b) lubricants, e.g. silica, talcum, stearicacid, its magnesium or calcium salt and/or polyethyleneglycol; fortablets also c) binders e.g. magnesium aluminum silicate, starch paste,gelatin, tragacanth, methylcellulose, sodium carboxymethylcelluloseand/or polyvinylpyrrolidone; if desired d) disintegrants, e.g. starches,agar, alginic acid or its sodium salt, or effervescent mixtures; and/ore) absorbents, colorants, flavors and sweeteners. Injectablecompositions are preferably aqueous isotonic solutions or suspensions,and suppositories are advantageously prepared from fatty emulsions orsuspensions. Said compositions may be sterilized and/or containadjuvants, such as preserving, stabilizing, wetting or emulsifyingagents, solution promoters, salts for regulating the osmotic pressureand/or buffers. In addition, they may also contain other therapeuticallyvaluable substances. Said compositions are prepared according toconventional mixing, granulating or coating methods, respectively, andcontain about 0.1 to 75%, preferably about 1 to 50%, of the activeingredient.

Suitable formulations for transdermal application include an effectiveamount of a compound of formula I with carrier. Advantageous carriersinclude absorbable pharmacologically acceptable solvents to assistpassage through the skin of the host. Characteristically, transdermaldevices are in the form of a bandage comprising a backing member, areservoir containing the compound optionally with carriers, optionally arate controlling barrier to deliver the compound to the skin of the hostat a controlled and predetermined rate over a prolonged period of time,and means to secure the device to the skin.

The invention also relates to a method of blocking theN-methyl-D-aspartate excitatory amino acid receptor in mammals, and to amethod of treatment of disorders in mammals, e.g. such responsive toblockade of the N-methyl-D-aspartate excitatory amino acid receptor,such as cerebral ischemia, convulsive disorders and anxiety, using aneffective amount of a compound of the invention as a pharmacologicallyactive substance, preferably in the form of above-cited pharmaceuticalcompositions.

A particular embodiment thereof relates to a method of treating cerebralischemia and of inhibiting brain damage resulting from cerebral ischemia(in a stroke) in mammals which comprises the administration to a mammalin need thereof of an effective amount of an N-methyl-D-aspartateblocking compound of the invention or of a pharmaceutical compositioncomprising a said compound.

The dosage of active compound administered is dependent on the speciesof warm-blooded animal (mammal), the body weight, age and individualcondition, and on the form of administration.

A unit dosage for a mammal of about 50 to 70 kg may contain betweenabout 5 and 100 mg of the active ingredient.

The following examples are intended to illustrate the invention and arenot to be construed as being limitations thereon. Temperatures are givenin degrees Centigrade. If not mentioned otherwise, all evaporations areperformed under reduced pressure, preferably between about 15 and 100 mmHg.

EXAMPLE 1

A mixture of 1.19 g of 4-(diethylphosphonomethyl)-2-pyridinecarboxamideand 0.75 g of platinum oxide in 30 ml of acetic acid is hydrogenated at3 atmospheric pressure for 6 hours at room temperature. The reactionmixture is filtered and the solvent is removed in vacuo. The residue isdissolved in methylene chloride and washed with a small volume ofsaturated sodium bicarbonate solution. After drying over magnesiumsulfate, a methylene chloride solution of a 2:1 mixture of cis and trans4-(diethylphosphonomethyl)-2-piperidinecarboxamide is obtained. After 3days at room temperature this mixture isomerizes to the more stable cisisomer. Removal of the solvent in vacuo affordscis-4-(diethylphosphonomethyl)-2-piperidinecarboxamide as an oil, whichis converted to the hydrochloride salt, melting at 155°-158°.

The starting material is prepared as follows:

A mixture of 2.2 g of 4-(diethylphosphonomethyl)pyridine [Roczniki Chem.38, (4), 625 (1964); Chem. Abst. 61, 10703], 2.2 g of m-chloroperbenzoicacid and 30 ml of chloroform is stirred at room temperature for 16hours. The solvent is removed in vacuo and water is added. After washingthe aqueous layer with ether, the water is removed in vacuo to afford4-(diethylphosphonomethyl)pyridine-N-oxide.

A mixture of 1.2 g of 4-(diethylphosphonomethyl)pyridine-N-oxide, 1.35ml of triethylamine and 2.6 ml of trimethylsilylcyanide is heated at 90°for 1 hour. The volatiles are removed in vacuo and the residue isdissolved in ethyl acetate and washed with a small volume of aqueoussodium bicarbonate. After drying over magnesium sulfate the solvent isremoved in vacuo to afford 2-cyano-4-(diethylphosphonomethyl)pyridine asan oil.

A mixture of 1.10 g of 2-cyano-4-(diethylphosphonomethyl)pyridine and4.5 ml of concentrated sulfuric acid is heated at 90° for 5 minutes. Thereaction mixture is poured onto ice and neutralized with 10% sodiumhydroxide. The resulting precipitate is collected to afford4-(diethylphosphonomethyl)-2-pyridinecarboxamide melting at 140°-142°.

EXAMPLE 2

A solution of 3.0 g ofcis-4-(diethylphosphonomethyl)-2-piperidinecarboxamide in 90 ml of 20%hydrochloric acid is heated under reflux with stirring for 16 hours.After removal of the solvent, the residue is crystallized from ethylacetate/ethanol to afford cis-4-phosphonomethyl-2-piperidinecarboxylicacid hydrochloride, melting at 284°-285° (dec).

EXAMPLE 3

A mixture of 330 mg of 4-phosphonomethyl-2-pyridinecarboxylic acid, 150mg of platinum oxide, 20 ml of acetic acid and 100 ml of water ishydrogenated at 3 atmospheres pressure at room temperature for 20 hours.The solvent is removed in vacuo to afford a 2:1 mixture of cis and trans4-phosphonomethyl-2-piperidinecarboxylic acid. The residue is dissolvedin aqueous hydrochloric acid and the solvent removed in vacuo to afforda 2:1 mixture of cis and trans 4-phosphonomethyl-2-piperidinecarboxylicacid hydrochloride melting at 145° (dec).

The starting material was prepared as follows:

A mixture of 350 mg of 2-cyano-4-diethylphosphonomethylpyridine and 10ml of 20% hydrochloric acid is refluxed for 16 hours. After removal ofthe solvent in vacuo the residue is triturated with 95% ethanol toafford 4-phosphonomethyl-2-pyridinecarboxylic acid melting at 265°-268°(dec).

EXAMPLE 4

Prepared essentially according to the procedures described in theprevious examples are:

a) cis and trans 5-phosphonomethyl-2-piperidinecarboxylic acidhydrochloride, m.p. above 250°;

b) cis and trans 3-phosphonomethyl-2-piperidinecarboxylic acidhydrochloride, m.p. above 250°;

c) cis 3-(2-phosphonoethyl)-2-piperidinecarboxylic acid, m.p. 160°-190°dec.

d) cis-5-(2-phosphonoethyl)-2-piperidinecarboxylic acid hydrochloride,m.p. 125° dec.

e) cis 4-(2-phosphonoethyl)-2-piperidinecarboxyli acid;

f) cis 4-(3-phosphonopropyl)-2-piperidinecarboxylic acid, m.p. 287° dec.

g) cis 4-(1-methyl-1-phosphonoethyl)-2-piperidinecarboxylic acidhydrochloride, m.p. 250° (dec).

h) cis 4-(1-phosphonoethyl)-2-piperidinecarboxylic acid, m.p. 220° dec,e.g. via 4-(1-phosphonoethyl)-2-pyridinecarboxylic acid, m.p. 264°-265°dec.

i) 5-(3-phosphonopropyl)-2-piperidinecarboxylic acid e.g. via5-(3-phosphonopropyl)-2-pyridinecarboxylic acid hydrochloride, m.p.210°-220° dec.

j) cis 3-(3-phosphonopropyl)-2-piperidinecarboxylic acid, via3-(3-phosphonopropyl)-2-pyridinecarboxylic acid, m.p. 230°-235° dec.

k) 3-methyl-4-phosphonomethyl-2-piperidinecarboxylic acid, m.p. 325°dec., starting from 3-methyl-4-chloromethylpyridine via reduction of3-methyl-4-phosphonomethylpyridinecarboxylic acid.

1) cis-6-methyl-4-phosphonomethyl-2-piperidinecarboxylic acid, m.p.260°-265°, starting from 2-methyl-4-chloromethylpyridine.

m) cis-5-methyl-4-phosphonomethyl-2-piperidinecarboxylic acid, m.p.above 250°, starting from 3-methyl-4-chloromethylpyridine via reductionof 5-methyl-4-phosphonomethyl-2-pyridinecarboxylic acid, m.p. 295° dec.

Certain starting materials are prepared as follows:

1. Treatment of 3-(diethylphosphonomethyl)pyridine (Biochemistry 19,3400) with m-chloroperbenzoic acid followed by trimethylsilyl cyanidegives both 3-(diethylphosphonomethyl)-2-cyanopyridine and5-(diethylphosphonomethyl)-2-cyanopyridine, the starting materials forcompounds under a) and b).

2. Similarly, 3-(2-diethylphosphonoethyl)pyridine (Biochemistry 19,3400) is converted to the corresponding starting materials for compoundsunder c) and d); 4-(2-diethylphosphonoethyl)pyridine (Chem. Abstracts89, 35665) is converted to 4-(2-diethylphosphonoethyl)-2-cyanopyridine,the starting material for compound under e).

3. Reaction of 3-(4-pyridinyl)propyl chloride with diethyl phosphite(diethyl phosphonate) and sodium hydride in toluene yields4-(3-diethylphosphonopropyl)pyridine which is converted according to theprocedure described hereinabove to4-(3-diethylphosphonopropyl)-2-cyanopyridine, the starting material forcompound under f).

4. A mixture of 1.0 g of 4-(diethylphosphonomethyl)pyridine and 0.5 g of50% sodium hydride in 4 ml of dimethylformamide and 16 ml oftetrahydrofuran is heated under reflux for 30 minutes. Methyl iodide(0.52 ml) is added and heating under reflux is continued for 30 minutes.The reaction mixture is evaporated to dryness and the residue ischromatographed on silica gel with methanol/methylene chloride (1:10) asthe eluant to give 4-(1-methyl-1-diethylphosphonoethyl)-pyridine whichis converted to 2-cyano-4-(1-methyl-1-diethylphosphonoethyl)pyridine,the starting material for compound under g).

5. Similarly treatment of 4-(diethylphosphonomethyl)pyridine as abovewith 1 mole equivalent of methyl iodine yields4-(1-diethylphosphonoethyl)pyridine, the starting material for compoundunder h).

EXAMPLE 5

a) A solution of 370 mg of cis-4-phosphonomethyl-2-piperidinecarboxylicacid in 15 ml of saturated ethanolic hydrochloric acid is heated underreflux for 16 hours. The solvent is removed in vacuo. A solution of theresidue in ethanol is treated with 0.21 ml of propylene oxide andevaporated to dryness to yieldcis-4-phosphonomethyl-2-piperidinecarboxylic acid ethyl ester, m.p.230°-235° dec.

Similarly prepared are:

b) cis-4-phosphonomethyl-2-piperidinecarboxylic acid methyl ester, m.p.198°-200°;

c) cis-4-phosphonomethyl-2-piperidinecarboxylic acid n-butyl ester, m.p.241°-244°;

d) cis-4-(3-phosphonopropyl-2-piperidinecarboxylic acid ethyl ester,m.p. 197°-202°;

e) cis-4-phosphonomethyl-2-piperidinecarboxylic acid n-propyl ester,m.p. 245°-249°;

f) cis-4-phosphonomethyl-2-piperidinecarboxylic acid isobutyl ester,m.p. 254°-259°.

EXAMPLE 1

a) A solution of 278 mg ofcis-4-diethylphosphonomethyl-2-piperidinecarboxamide in 5 ml ofmethylene chloride to which is added 0.43 ml of trimethylsilyl iodide isstirred at room temperature for 16 hours. The mixture is evaporated todryness, the residue is dissolved in water, and the solution isevaporated to dryness. A solution of the resulting solid in ethanol istreated with 0.21 ml of propylene oxide to yieldcis-4-phosphonomethyl-2-piperidinecarboxamide, m.p. 295°-298° dec.

EXAMPLE 7

a) To a solution of 200 mg ofcis-4-phosphonomethyl-2-piperidinecarboxylic acid, 96 mg of sodiumcarbonate in 5 ml of water and 2.31 ml of 1N aqueous sodium hydroxide isadded 119 mg of benzoyl chloride. The reaction mixture is stirred atroom temperature for 16 hours and the solvent is removed in vacuo. Theresidue is dissolved in ethanol, the solution is filtered and evaporatedto dryness. Crystallization from ethanol/ethyl acetate affordscis-1-benzoyl-4-phosphonomethyl-2-piperidinecarboxylic acid, m.p.135°-145° dec.

b) Similarly prepared iscis-1-benzyloxycarbonyl-4-phosphonomethyl-2-piperidinecarboxylic acidmethyl ester.

c) Similarly prepared is cis1-(3-phenylpropionyl)-4-phosphonomethyl-2-piperidinecarboxamide, m.p.95°-100°, via cis 4-phosphonomethyl-2-piperidinecarboxamide.

EXAMPLE 8

A mixture of 357 mg ofcis-1-benzyloxycarbonyl-4-phosphonomethyl-2-piperdinecarboxylic acid,550 mg of diisopropylethylamine and 600 mg of chloromethyl pivalate in 2ml of dimethylformamide is heated at 80° for 2 hours. The reactionmixture is evaporated to dryness at 70°/0.1 mm Hg. The residue isdissolved in ethyl acetate, the solution is washed with water andevaporated to dryness to yieldcis-1-benzyloxycarbonyl-4-[di(pivaloyloxymethyl)phosphonomethyl]-2-piperidinecarboxylicacid pivaloyloxymethyl ester (after chromatography on silica gel usingether/methylene dichloride as the eluent). The product is dissolved in40 ml of ethanol and hydrogenated in the presence of 10% palladium oncharcoal to yieldcis-4-[di(pivaloyloxymethyl)-phosphonomethyl]-2-piperidinecarboxylicacid pivaloyloxymethyl ester.

The starting material is prepared by treatment ofcis-4-phosphonomethyl-2-piperidinecarboxylic acid with banzylchloroformate under standard amino acid acylation conditions, e.g. asdescribed in Example 7.

EXAMPLE 9

a) A mixture of 500 mg of4-(diethylphosphonomethyl)quinoline-2-carboxamide and 1 g of 10%palladium on charcoal in 75 ml of methanol is hydrogenated at 3atmospheres pressure for 24 hours, filtered and evaporated to dryness.Chromatography on silica gel using methanol/methylene chloride (1:10) aseluent yieldscis-4-(diethylphosphonomethyl)-1,2,3,4-tetrahydroquinoline-2-carboxamide.

The starting material is prepared as follows:

To a stirred solution of 10 g of 4-quinolinecarboxaldehyde in 400 ml ofabsolute ethanol at room temperature is added 2.4 g of sodiumborohydride. After 45 minutes, 20 ml of water is added and the reactionmixture is stirred for an additional 20 minutes. Acetic acid (20 ml) isadded slowly. The reaction mixture is evaporated to a small volume andpartitioned between water and methylene chloride. The organic layer iswashed with saturated potassium carbonate, saturated sodium chloridesolution, dried over sodium sulfate and evaporated to dryness. Theresidue is purified by chromatography on silica gel usingmethanol/methylene chloride (1:10) as eluent to yield4-hydroxymethylquinoline; R_(f) =0.59.

A solution of methanesulfonyl chloride (4.84 ml) in 20 ml of methylenechloride is slowly added over 20 minutes to a solution of 8.29 g of4-hydroxymethylquinoline and 11 ml of triethylamine in 200 ml ofmethylene chloride at 0°. After completion of the reaction at roomtemperature, the reaction mixture is partitioned between methylenechloride and saturated potassium carbonate solution. The organic layeris dried over sodium sulfate and evaporated to dryness to yield4-(methanesulfonyloxymethyl)quinoline as an oil.

To a solution of 1.62 g of sodium hydride (from 3.24 g of a 50% sodiumhydride dispersion in mineral oil) in 100 ml of toluene is addeddropwise a solution of 8 ml of diethyl phosphite in 20 ml of toluene.The reaction mixture is heated to 80°, a solution of the above obtained4-(methanesulfonyloxymethyl)-quinoline in 90 ml of toluene and 10 ml ofmethylene chloride is added. After 20 minutes a second portion of 1.2 gof sodium hydride is added and the reaction mixture is stirred for anadditional 10 minutes. The reaction mixture is then evaporated todryness, the product is partitioned between water and ethyl acetate. Theethyl acetate extract is washed with saturated sodium chloride solution,dried over sodium sulfate and evaporated to dryness. The residue ischromatographed on silica gel using methanol/methylene chloride (5:95)as eluent to yield 4-(diethylphosphonomethyl)quinoline; R_(f) =0.3.

To a solution of 5.7 g of 4-(diethylphosphonomethyl)quinoline in 100 mlof methylene chloride at room temperature is added 3.2 g ofm-chloroperbenzoic acid. After reacting for 45 minutes, an additional1.5 g portion of m-chloroperbenzoic acid is added, and the reactionmixture is stirred for one hour. The reaction mixture is washed withsaturated potassium carbonate solution, dried over sodium sulfate andevaporated to dryness to give4-(diethylphosphonomethyl)-quinoline-N-oxide.

A mixture of 5.9 g of 4-(diethylphosphonomethyl)-quinoline-N-oxide, 15ml of trimethylsilyl cyanide and 7 ml of triethylamine is heated at 80°for 1 hour and evaporated to dryness. The residue is purified bychromatography on silica gel using methanol/methylene chloride (5:95) aseluent to yield 4-(diethylphosphonomethyl)-2-cyanoquinoline as an oil.

A solution of 5.9 g of 4-(diethylphosphonomethyl)-2-cyanoquinoline in 24ml of concentrated sulfuric acid is heated at 80° for 5 minutes, cooledto 0° and added slowly to an ice-cooled mixture of 50 g of sodiumcarbonate in 50 ml of water and 100 ml of methylene chloride. Theorganic layer is separated, dried over sodium sulfate and evaporated todryness to yield 4-(diethylphosphonomethyl)quinoline-2-carboxamide.

b) Similarly prepared iscis-4-(3-diethylphosphonopropyl)-1,2,3,4-tetrahydroquinoline-2-carboxamide.

EXAMPLE 10

a) A solution of 220 mg ofcis-4-(diethylphosphonomethyl)-1,2,3,4-tetrahydroquinoline-2-carboxamidein 50 ml of 6N aqueous hydrochloric acid is heated under reflux for 14hours, and evaporated to dryness. The residue is dried under high vacuumat 100° for 48 hours to yieldcis-4-phosphonomethyl-1,2,3,4-tetrahydroquinoline-2-carboxylic acid,m.p. 171°-173°.

b) Similarly prepared iscis-4-(3-phosphonopropyl)-1,2,3,4-tetrahydroquinoline-2-carboxylic acidhydrochloride.

EXAMPLE 11

a) Treatment ofcis-4-phosphonomethyl-1,2,3,4-tetrahydroquinoline-2-carboxylic acidfirst with benzyl chloroformate and then with chloromethyl pivalateunder conditions essentially as described in example 8, including thehydrogenolysis, yields4-[di-(pivaloyloxymethyl)phosphonomethyl]-1,2,3,4-tetrahydroquinoline-2-carboxylicacid pivaloyloxymethyl ester.

b) Treatment ofcis-4-phosphonomethyl-1,2,3,4-tetrahydroquinoline-2-carboxylic acid withethanolic hydrochloric acid under conditions essentially as described inExample 5 yieldscis-4-phosphonomethyl-1,2,3,4-tetrahydroquinoline-2-carboxylic acidethyl ester.

EXAMPLE 12

A mixture of 400 mg of 4-phosphonomethylquinoline-2-carboxylic acidhydrochloride, 150 mg of platinum oxide, 20 ml of acetic acid and 100 mlof water is hydrogenated at 3 atmospheres pressure at room temperaturefor 20 hours to affordcis-4-phosphonomethylperhydroquinoline-2-carboxylic acid; HCl salt; m.p.230°-250° dec.

The starting material is prepared as follows:

A solution of 4-(diethylphosphonomethyl)quinoline-2-carboxamide with 6Nhydrochloric acid is heated under reflux overnight to yield4-phosphonomethyl-quinoline-2-carboxylic acid hydrochloride, m.p.218°-221°.

EXAMPLE 13

A mixture of 2.0 g of4-(diethylphosphonomethylidene)-N-t-butoxycarbonylpyrrolidine-2-carboxylicacid methyl and ethyl ester, and 800 mg of 10% palladium on charcoalcatalyst in 30 ml of ethanol is hydrogenated at 3 atmospheres pressureand room temperature for 18 hours. The reaction mixture is filtered freeof catalyst, the catalyst is washed with methylene chloride, thecombined filtrate is evaporated to dryness to yield a mixture ofN-t-butoxycarbonyl-4-diethylphosphonomethylpyrrolidine-2-carboxylic acidmethyl and ethyl esters.

The above product is treated with 10 ml trifluoroacetic acid for 5minutes, the trifluroacetic acid is removed under vacuum. A solution ofthe residue in 30 ml of 6N hydrochloric acid is heated under reflux for6 hours and evaporated to dryness. A solution of the residue in 15 mlethanol is treated with 1 ml of propylene oxide. The resultingprecipitate is filtered off to yield4-phosphonomethylpyrrolidine-2-carboxylic acid(4-phosphonomethylproline); NMR (D₂ O): 4.53, 3.82, 2.88, 2.80, 2.0 ppm;product is mixture of cis and trans compounds (about 9:1).

The starting material is prepared as follows:

A mixture of 10.0 g of 4-hydroxyproline, 13 ml of 6N sodium hydroxidesolution and 19.0 g of di-t-butyl dicarbonate is stirred vigorously atroom temperature for 24 hours. Concentrated hydrochloric acid (6.5 ml)is added and the reaction mixture is extracted with 30 ml of chloroform.The chloroform is discarded, the oil is separated from the aqueous layerto give N-t-butoxycarbonyl-4-hydroxyproline. A solution thereof in 70 mlof methanol is treated with ethereal diazomethane (prepared from 20 g ofN-methyl-N-nitrosourea, 60 ml of 40% aqueous potassium hydroxide and 200ml of ether) to give N-t-butoxycarbonyl-4-hydroxyproline methyl ester.

A mixture of 12.7 g of N-t-butoxycarbonyl-4-hydroxyproline methyl esterand 44.7 g of pyridinium chlorochromate in 150 ml of methylene chlorideis stirred at room temperature for 30 hours, diluted with 200 ml ofether and filtered through Florisil washing with ether (500 ml). Thesolution is evaporated to dryness, the residue is purified by flashchromatography on silica gel using ethyl acetate/hexane (40:60) aseluent to give N-t-butoxycarbonyl-4-oxoproline methyl ester.

A solution of 2.28M n-butyl lithium (4.6 ml) is added at -78° to asolution of 3.07 g of bis-(diethylphosphono)methane in 50 ml of drytetrahydrofuran. After 5 minutes, a solution of 2.5 g ofN-t-butoxycarbonyl-4-oxoproline methyl ester is added. The reactionmixture is heated under reflux for 20 hours. The volume is reduced to 20ml and the product is partitioned between methylene chloride and 2Nhydrochloric acid. The methylene chloride extract is dried andevaporated to dryness and the residue is purified by flashchromatography on silica gel eluting with methylene chloride/methanol(95:5) to obtain a mixture of4-(diethylphosphonomethylidene)-N-t-butoxycarbonylpyrrolidine-2-carboxylicacid methyl and ethyl esters.

EXAMPLE 14

Preparation of an injectable formulation containing 10 mg of the activeingredient per 5 ml of solution:

    ______________________________________                                        Formula                                                                       ______________________________________                                        cis-4-phosphonomethyl-2-piperidine-                                                                   10.0    g                                             carboxylic acid hydrochloride                                                 Propylparaben           0.5     g                                             Water for injection q.s.                                                                              5000.0  ml                                            ______________________________________                                    

The active ingredient and preservative are dissolved in 3500 ml of waterfor injection and the solution is diluted to 5000 ml. The solution isfiltered through a sterile filter and filled into injection vials understerile conditions each vial containing 5 ml of the solution.

EXAMPLE 15

A solution of 2.0 g ofcis-1-benzyloxycarbonyl-4-phosphonomethyl-2-piperidinecarboxylic acid in10 ml of methylene chloride is treated with ethereal diazomethane untila persistent yellow color is obtained. After removal of solvent thetriester is heated at 50° in 10 ml of tetrahydrofuran and 10 ml of 1Nsodium hydroxide. After acidification the product is extracted withether, the organic layer dried and evaporated to yieldcis-1-benzyloxycarbonyl-4-dimethylphosphonomethyl-2-piperidinecarboxylicacid.

EXAMPLE 16

A solution of 1.0 g ofcis-1-benzyloxycarbonyl-4-dimethylphosphonomethyl-2-piperidinecarboxylicacid in 30 ml of ethanol is hydrogenated at 3 atmospheres pressure over500 mg of 10% palladium on carbon catalyst in 30 ml of ethanol.Filtration and removal of solvent affordscis-4-dimethylphosphonomethyl-2-piperidine-carboxylic acid as anamorphous solid.

EXAMPLE 17

A solution of 3.38 g ofcis-1-benzyloxycarbonyl-4-dimethylphosphonomethyl-2-piperidinecarboxylicacid in 35 ml of methylene chloride is treated with 1.42 g of1,1'-carbonyldiimidazole and 1.3 g of (+)-alpha-methylbenzylamine. Afterstirring for 16 hours, the reaction mixture is washed with 1Nhydrochloric acid and saturated sodium bicarbonate solution, dried, andthe solvent removed. Separation of the resulting diastereomers by highpressure liquid chromatography (HPLC) using a reverse phase C₁₈ columnand acetonitrile/water (2:3) as eluent affords the two diastereomers ofcis-1-benzyloxycarbonyl-4-dimethylphosphonomethyl-2-piperidine-(N-1-phenylethyl)carboxamide.

Hydrogenation of the first eluted diastereomer in ethanol with palladiumon charcoal catalyst for 4 hours at 3 atmospheres pressure affords thecorrespondingcis-4-dimethylphosphonomethyl-2-piperidine-(N-1-phenylethyl)-carboxamide.Treatment with 6N hydrochloric acid under reflux for 24 hours affords(-)-cis-4-phosphonomethyl-2-piperidinecarboxylic acid, [α]_(D) ²⁵=-5.93° (H₂ O), the pharmacologically more active enantiomer of thecompound of Example 2.

The corresponding (+)-cis-4-phosphonomethyl-2-piperidinecarboxylic acid,the less active enantiomer, is similarly obtained.

EXAMPLE 18

A mixture of 600 mg ofcis-1-benzyloxycarbonyl-4-dimethylphosphonomethyl-2-piperidinecarboxylicacid methyl ester in 10 ml of methylene chloride is treated with 538 mgof trimethylsilyl iodide at room temperature to yield cis1-benzyloxycarbonyl-4-phosphonomethyl-2-piperidinecarboxylic acid methylester as an oil.

EXAMPLE 19

A mixture of 500 mg ofcis-4-diethylphosphonomethyl-2-piperidinecarboxamide, 3 ml of 37%aqueous formaldehyde, 50 ml of methanol and 500 mg of 10% palladium oncarbon catalyst is hydrogenated at 3 atmospheres pressure for 16 hours.The solvent is removed and the residue chromatographed on silica gelwith 10% methanol/methylene chloride as the eluent to affordcis-1-methyl-4-diethylphosphonomethyl-2-piperidinecarboxamide. Thisproduct is refluxed for 16 hours in 6N hydrochloric acid followed bytreatment with propylene oxide to yield cis1-methyl-4-phosphonomethyl-2-piperidinecarboxylic acid, m.p. 256°-260°.

EXAMPLE 20

A solution of 1.0 g of cis4-diethylphosphonomethyl-2-piperidinecarboxylic acid ethyl ester isreacted with 552 mg of N-t-butoxycarbonylglycine in the presence ofN,N'-dicyclohexyl-carbodiimide in 10 ml of methylene chloride of roomtemperature for 16 hours to yield cis1-[alpha-(t-butoxycarbonylamino)acetyl]-4-diethylphosphonomethyl-2-piperidinecarboxylicacid ethyl ester as an oil. Treatment with trimethylsilyl iodide yieldscis 1-(alpha-aminoacetyl)-4-phosphonomethyl-2-piperidinecarboxylic acidethyl ester, m.p. 150°-155° dec.

EXAMPLE 21

a) MethylN-t-butoxycarbonyl-4-(diethylphosphonoethyl)pyrrolidine-2-carboxylate(0.45 g) is hydrolyzed as described in Example 13 to yield cis4-(2-phosphonoethyl)pyrrolidine-2-carboxylic acid; NMR (D₂ O): 4.22,3.45, 2.95, 2.54, 2.4 ppm (1 H each).

The starting material is prepared as follows:

To a suspension of 3.44 g of benzyloxycarbonylmethyltriphenylphosphoniumbromide in 20 ml of tetrahydrofuran is added 10 ml 0.65M potassiumhexamethyldisilazide solution in toluene followed by 1.5 gN-t-butoxycarbonyl-4-oxoproline methyl ester in 4 ml of tetrahydrofuran.After refluxing for 72 hours the solvent is evaporated and the residueflash chromatrographed with ethyl acetate/hexane (20:80) to afford amixture of cis and trans (mostly cis) methylN-t-butoxycarbonyl-4-(2-oxo-2-benzyloxyethylidene)-pyrrolidine-2-carboxylate.

A solution of 0.58 g of the above product in 15 ml of methanol ishydrogenated at 3 atmospheres pressure for 3 hours in the presence of400 mg of 10% Pd/C. The reaction mixture is filtered through Celite, thesolvent evaporated and the residue flash chromatographed withmethanol/methylene chloride (10:90) to afford cis methylN-t-butoxycarbonyl-4-(carboxymethyl)pyrrolidine-2-carboxylate.

To 0.67 g of cis methylN-t-butoxycarbonyl-4-(carboxymethyl)-pyrrolidine-2-carboxylate in 1 mlTHF is added at 0° 3.5 ml of borane (1M) in THF. After stirring 0.5hour, 1 ml of water is added, the solvent is evaporated and the residueis flash chromatographed with ethyl acetate/hexane (75:25) to afford cismethyl N-t-butoxycarbonyl-4-(2-hydroxyethyl)-pyrrolidine-2-carboxylate.

To a solution of 0.58 g of cis methylN-t-butoxycarbonyl-4-(2-hydroxyethyl)pyrrolidine-2-carboxylate in 6 mlmethylene chloride is added at 0° 0.577 g triphenylphosphine followed by0.388 g N-bromosuccinimide. After stirring 0.5 hour, the solvent isevaporated and the residue flash chromatographed using ethylacetate/hexane (35:65) to afford cis methylN-t-butoxycarbonyl-4-(2-bromoethyl)-pyrrolidine-2-carboxylate.

A mixture of 0.60 g of cis methylN-t-butoxycarbonyl-4-(2-bromoethyl)pyrrolidine-2-carboxylate and 3 mltriethyl phosphite is refluxed for 2 hours. The excess triethylphosphite is distilled off under vacuum and the residue is flashchromatographed with methylene chloride/methanol (95:5) to afford cismethylN-t-butoxycarbonyl-4-(2-diethylphosphonoethyl)pyrrolidine-2-carboxylate.

b) Similarly obtained is(+)-cis-4-(2-phosphonoethyl)pyrrolidine-2-carboxylic acid, [α]_(D) ²⁵=+23.7°, starting with the D-proline derivative.

c) Similarly prepared is cis3-(2-phosphonoethyl)pyrrolidine-2-carboxylic acid; NMR (D₂ O): 4.34,3.57, 3.35, 2.67 and 2.27 (1H each), 1.79 (4H), 1.52 (1H).

d) Similarly prepared is trans 3-(2-phosphonoethyl)pyrrolidine-2-carboxylic acid; NMR (D₂ O) 3.88, 3.44, 3.31, 2.47, 2.24(1H each), 1.71 (4H), 1.45 (1H).

The starting material for the trans product d) is prepared as follows:

A solution of 1.25 g of ethyl3-(2-oxo-2-benzyloxyethylidene)-1-ethoxycarbonylpyrrolidine-2-carboxylate(obtained according to the procedure described under a) in 10 ml ofanhydrous ethanol containing one equivalent of lithium ethoxide isheated under reflux for seven days. One equivalent of 1N hydrochloricacid is added to the cooled solution, which is then concentrated,diluted with 20 ml water and extracted with three 20 ml portions atmethylene chloride. The extracts are dried over sodium sulfate, filteredand concentrated. The residue is chromatographed under high pressureeluting with ethyl acetate/hexane (5:95) to afford trans ethyl3-(2-oxo-2-benzyloxyethylidene)-1-ethoxycarbonylpyrrolidine-2-carboxylate(in addition to approximately an equal amount at the cis isomer) whichis converted to trans ethyl1-ethoxycarbonyl-3-(diethylphosphonoethyl)-pyrrolidine-2-carboxylateessentially as described under a).

EXAMPLE 22

a) A stirred solution of 5.3 ml of bis-(diethylphosphono)methane in 30ml of anhydrous tetrahydrofuran (THF) under nitrogen is cooled to -78°and 8.5 ml of 2.5M butyl lithium is added dropwise. After stirring 5minutes a solution of 4.64 g of ethyl1-ethoxycarbonyl-3-oxopyrrolidine-2-carboxylate [J. Am. Chem. Soc. 86,5297 (1964)] in 30 ml dry THF is added dropwise rapidly. The solution isheated at reflux for 18 hours, cooled to room temperature andconcentrated; 40 ml of 1N hydrochloric acid is added and the mixture isextracted with 100 ml of methylene chloride. The organic fraction iswashed with 25 ml water, dried over Na₂ SO₄ filtered and concentrated.Purification by flash chromatography using ethyl acetate as solventyields ethyl1-ethoxycarbonyl-3-(diethylphosphonomethyl)-2,5-dihydropyrrole-2-carboxylate.

EXAMPLE 23

A solution of 2.75 g of ethyl1-ethoxycarbonyl-3-(diethylphosphonomethyl)-2,5-dihydropyrrole-2-carboxylatein 35 ml ethyl alcohol and 1.5 g 10% Pd/C is hydrogenated at 3atmospheres pressure to yield cis and trans ethyl1-ethoxycarbonyl-3-(diethylphosphonomethyl)-pyrrolidine-2-carboxylate.

EXAMPLE 24

a) A solution of 2.7 g of cis and trans ethyl1-ethoxycarbonyl-3-(diethylphosphonomethyl)pyrrolidine-2-carboxylate isheated under reflux with 6N hydrochloric acid for 6 hours to yield3-(phosphonomethyl)-pyrrolidine-2-carboxylic acid hydrochloride; NMR (D₂O): 4.78, 4.40, 3.95, 3.83, 3.72, 3.20, 3.01, 2.78, 2.69 ppm.

b) Similarly hydrolysis of ethyl1-ethoxycarbonyl-3-(diethylphosphonomethyl)-2,5-dihydropyrrole-2-carboxylateaffords 3-(phosphonomethyl)-2,5-dihydropyrrole-2-carboxylic acidhydrochloride which on treatment with propylene oxide yields the freeamino acid, m.p. 215° dec.

EXAMPLE 25

Ethyl4-[1-(3-diethylphosphonoprop-2-enyl)]-1-tert-butoxycarbonylpiperidine-2-carboxylateis hydrolyzed with 6N hydrochloric acid to yield4-[1-(3-phosphonoprop-2-enyl)]piperidine-2-carboxylic acid.

The starting material is prepared as follows:

4-(2-hydroxyethyl)-pyridine is oxidized to4-(2-hydroxyethyl)-pyridine-N-oxide which is in turn treated withtrimethylsilyl cyanide to yield 4-(2-hydroxyethyl)-2-cyanopyridine whichis converted to ethyl 4-(2-hydroxyethyl)-2-pyridine carboxylate and thenhydrogenated to yield ethyl 4-(2-hydroxyethyl)-piperidine-2-carboxylate.

A solution of 2.01 g of ethyl 4-(2-hydroxyethyl)piperidine-2-carboxylatein 5 ml methylene chloride is added to a solution of 2.20 g ofdi-tert-butyl dicarbonate in 10 ml methylene chloride. After standingfor 10 minutes the solvent is evaporated and the residue is flashchromatographed with hexane: ethyl acetate (50:50) to afford ethyl4-(2-hydroxyethyl)-1-tert-butoxycarbonylpiperidine-2-carboxylate.

To a solution of 1.56 g of dimethyl sulfoxide in 10 ml methylenechloride is added 2.2 g of oxalyl chloride at -78°. After 20 minutes 2.4g ofethyl(2-hydroxyethyl)-1-tert-butoxycarbonyl-piperidine-2-carboxylate in5 ml methylene chloride is added. The reaction is stirred for one hourand 2.2 g of triethylamine is added. The ice bath is removed, thesolvent evaporated and the residue is flash chromatographed with hexane:ethyl acetate (70:30) to afford ethyl1-tert-butoxycarbonylpiperidine-2-carboxylate-4-acetaldehyde.

At -78°, 2.73 ml n-butyllithium (2.5 ) is added to 2.02 gbis(diethylphosphono)-methane in 20 ml anhydrous tetrahydrofuran. After5 minutes 2.08 g of ethyl1-tert-butoxycarbonylpiperidine-2-carboxylate-4-acetaldehyde in 5 mltetrahydrofuran is added. The mixture is then refluxed for 16 hours. Thecooled reaction mixture is concentrated and flash chromatographed (95:5methelene chloride:methanol) to yield ethyl4-[1-(3-diethylphosphonoprop-2-enyl)]-1-tert-butoxycarbonylpiperidine-2-carboxylate.

EXAMPLE 26

The following compounds can be prepared according to methods generallyillustrated in the previous examples:

(a) trans 3-[1-(4-phosphonobut-3-enyl)]-pyrrolidine-2-carboxylic acid;

(b) trans 3-[1-(4-phosphonobut-2-enyl)]-pyrrolidine-2-carboxylic acid;

(c) trans 3-[1-(4-phosphonobutyl]-pyrrolidine-2-carboxylic acid (byhydrogenation of double bond in compound of example (a) above).

The starting material for compound (a) can be prepared as follows:

Trans ethyl N-ethoxycarbonyl-pyrrolidine-2-carboxylate-3-acetaldehyde iscondensed with (C₆ H₅)₃ P=CHOCH₃ under conditions of the Wittig reactionto afford trans ethylN-ethoxycarbonylpyrrolidine-2-carboxylate-3-propionaldehyde.Condensation with bis-(diethylphosphono)methane under conditionsdescribed herein (e.g. example 25) yields trans ethyl3-[1-(4-diethylphosphonobut-3-enyl)]-pyrrolidine-2-carboxylate.

The starting material for compound (b) can be prepared as follows:

The alcohol, trans ethylN-ethoxycarbonyl-3-(2-hydroxyethyl)-pyrrolidine-2-carboxylate isoxidized to the aldehyde, trans ethylN-ethoxycarbonylpyrrolidine-2-carboxylate-3-acetaldehyde, which iscondensed with triphenylphosphoranylideneacetaldehyde under conditionsof the Wittig reaction; the resulting α,β-unsaturated C₄ -aldehyde isreduced to the corresponding alcohol which is converted to the bromide.Condensation with triethyl phosphite yields ethyl3-[1-(4-diethylphosphonobut-2-enyl)]-pyrrolidine-2-carboxylate.

(d) 4-[1-(3-Phosphonoprop-1-enyl)]piperidine-2-carboxylic acid can besimilarly prepared using ethyl4-hydroxymethyl-N-ethoxycarbonylpiperidine-2-carboxylate asintermediate.

EXAMPLE 27

a) A mixture of 348 mg of 3-phosphonopyridine-2-carboxylic acidhydrochloride and 100 mg of Adams catalyst in dilute aqueous acetic acidis hydrogenated at 3 atmospheres pressure and room temperature to yield3-phosphonopiperidine-2-carboxylic acid, mp 150° dec.

The starting material is prepared as follows:

A solution of 1.5 g of 3-diethylphosphonopyridine, Bull. Chem. Soc. Jap.55, 909 (1982), in 20 ml of methylene chloride is treated with 2.33 gm-chloroperbenzoic acid at room temperature. The reaction mixture isallowed to stir at room temperature overnight, then concentrated undervacuum. The residue is partitioned between ether and water, the aqueouslayer is concentrated under vacuum to afford3-(diethylphosphono)-pyridine-N-oxide as a yellow oil.

A solution of 1.2 g of the above intermediate in 5 ml CHCl₃ is treatedwith 3.0 ml triethylamine and 3.0 ml trimethylsilyl cyanide and heatedunder reflux under N₂ atmosphere for 15 hours. The reaction mixture isthen cooled to room temperture, concentrated under vacuum, and theresidue is partitioned between ethyl acetate and 0.1N NaOH. The organiclayer is washed with saturated sodium chloride solution and dried overanhydrous magnesium sulfate. The crude product mixture is separated byflash column chromatography on silica gel, eluting with ethyl acetate:hexane (1:1) containing 1% methanol, to yield2-cyano-3-diethylphosphonopyridine and2-cyano-2-diethylphosphonopyridine.

A solution of 690 mg of 2-cyano-3-diethylphosphonopyridine in 8Nhydrochloric acid is heated under reflux for 14 hours. The solvent isremoved under vacuum and residue triturated with ethanol, filtered, anddried under vacuum to afford 3-phosphonopyridine-2-carboxylic acidhydrochloride, m.p. 251°-255°.

b) Similarly prepared is 5-phosphonopiperidine-2-carboxylic acidstarting with 2-cyano-5-diethylphosphonopyridine which is prepared asdescribed under a).

EXAMPLE 28

At -78°, 20.3 ml of butyllithium (1.64M) is added to 8.5 ml oftetraethylmethylenediphosphonate [bis(diethylphos phono)-methane] in 100ml anhydrous tetrahydrofuran. After 5 minutes, 9.26 g of1-tert-butoxycarbonyl-2-ethoxycarbonyl piperidine-4-acetaldehyde in 125ml anhydrous tetrahydrofuran is added. Mixture is refluxed 18 hours,cooled, concentrated and purified by flash chromatography using ethylacetate/hexane (75:25 to 9:1) to yield ethyl4-[1-(3-diethylphosphonoprop-2-enyl)]-1-(tert-butoxycarbonyl)-piperidine-2-carboxylate.

The starting material is prepared as follows:

A solution of 4-pyridylacetic acid in 500 ml of anhydrous ethanolcontaining 75 ml of concentrated sulfuric acid is refluxed 18 hours. Thesolution is cooled to 0° an neutralized by addition of sodium hydroxidesolution and saturated aqueous sodium carbonate. Extraction with ethylacetate yields on concentration in vacuo ethyl 4-pyridylacetate.

A solution of 23.8 g of ethyl 4-pyridylacetate in 100 ml of anhydroustetrahydrofuran is added dropwise to 5.5 g of lithium aluminum hydridein 150 ml of anhydrous tetrahydrofuran under nitrogen. The mixture isheated at 50° (bath) for 40 minutes, then cooled in an ice bath, and theexcess lithium aluminum hydride is decomposed by addition of 6.6 ml ofwater followed by 6.6 ml of 15% aqueous sodium hydroxide and 20 ml ofwater. The solid is filtered off and the filtrate concentrated in vacuoto yield 4-pyridylethanol.

A solution of 16.3 g of 4-pyridylethanol, 21.8 g ofchloro-tert-butyl-dimethylsilane and 10.9 g of imidazole in 150 ml ofdimethylformamide is stirred 1 hour at room temperature. The product isisolated by extraction into ethyl acetate/hexane (1:1) and washed 4times with 400 ml of water; the extract is filtered through silica geland concentrated in vacuo to yield4-(tert-butyl-dimethylsilyloxyethyl)-pyridine.

To a stirred solution of 28.8 g of4-(tert-butyldimethylsilyloxyethyl)-pyridine in 300 ml of methylenechloride is added 24 g of m-chloroperbenzoic acid. After 4 hours thesolution is washed with aqueous sodium carbonate solution and water. Thesolution is dried over sodium sulfate, filtered and concentrated invacuo to yield 4-(tert-butyl-dimethylsilyloxyethyl)-pyridine-N-oxide.

A solution of 28.6 g of4-(tert-butyl-dimethylsilyloxyethyl)-pyridine-N-oxide, 60.3 ml oftrimethylsilyl cyanide and 31.5 ml triethylamine is stirred undernitrogen at reflux for 3 hours. The dark solution is cooled in an icebath, 30 ml of ethanol added, followed by 400 ml ethyl acetate and 200ml hexane. The solution is washed twice with 150 ml of water, dried oversodium sulfate, filtered, concentrated in vacuo and purified by flashchromatography using ethyl acetate/hexane (1:10) to yield4-(tert-butyl-dimethylsilyloxyethyl)-2-cyanopyridine.

A solution of 22.2 g of4-(tert-butyl-dimethylsilyloxyethyl)-2-cyanopyridine in 220 ml anhydrousethanol containing 0.19 g of sodium is stirred at room temperature for24 hours. The solution is then cooled to 0° and 22 ml of 6N hydrochloricacid added. The solution is stirred at room temperature for 16 hours,cooled to 0° and 7.5 ml 6N sodium hydroxide added followed by 75 mlsaturated aqueous sodium bicarbonate. Extraction with methylene chlorideand flash chromatography using ethyl acetate yields ethyl4-(2-hydroxyethyl)-pyridine-2-carboxylate.

A mixture of 8.37 g of ethyl 4-(2-hydroxyethyl)-pyridine-2-carboxylatein 130 ml acetic acid and 4 g platinum oxide is hydrogenated at 50lbs/in². Filtration, concentration in vacuo, neutralization withpotassium carbonate and extraction with methylene chloride yields an oilthat is purified by flash chromatography using methylenechloride/methanol saturated with ammonia (20:1) to yield ethyl4-(2-hydroxyethyl)-piperidine-2-carboxylate.

A solution of 7.9 g ofethyl-4-(2-hydroxyethyl)-piperidine-2-carboxylate, 9.0 g di-tert-butyldicarbonate in 80 ml of methylene chloride is stirred for 2 hours atroom temperature and then concentrated in vacuo to yield ethyl1-(tert-butoxycarbonyl)-4-(2-hydroxyethyl)-piperidine-2-carboxylate.

A solution of 11.8 g of ethyl1-tert-butoxycarbonyl-4-(2-hydroxyethyl)-piperidine-2-carboxylate and12.6 g of pyridinium chlorochromate in 175 ml methylene chloride isstirred under nitrogen at room temperature for 80 minutes. Mixture isfiltered and purified by flash chromatography using ethyl acetate/hexane(25:75) to yield1-(tert-butoxycarbonyl)-2-ethoxycarbonyl-piperidine-4-acetaldehyde.

EXAMPLE 29

A mixture of 4.67 g of ethyl4-[1-(3-diethylphosphonoprop-2-enyl]-1-tert-butoxycarbonyl-piperidine-2-carboxylateand 75 ml 6N hydrochloric acid is refluxed 12 hours. The solution isconcentrated in vacuo to dryness. The residue is dissolved in 50 mlethanol and 3.8 ml of propylene oxide added. The solid that separates isfiltered off and dried in vacuo to yieldcis-4-[1-(3-phosphonoprop-2-enyl]-piperidine-2-carboxylic acid, m.p.163°-165°.

EXAMPLE 30

At -78°, 6.9 ml of butyllithium (1.6M) is added to 2.9 ml oftetraethylmethylene diphosphonate in 30 ml anhydrous tetrahydrofuran.After 5 minutes, 2.47 g of trans ethyl1-acetyl-piperidine-2-carboxylate-4-acetaldehyde in 55 mltetrahydrofuran (anhydrous) is added. The mixture is refluxed 18 hours,cooled, concentrated and purified by flash chromatography usingmethylene chloride/ethanol (100:3) to yield trans ethyl4-[1-(3-diethylphosphonoprop-2-enyl)]-1-acetyl-piperidine-2-carboxylate.

The starting material is prepared as follows:

At 0°, 9.4 ml acetic anhydride is added to a stirred solution of 13.5 gof ethyl 4-(2-hydroxyethyl)-piperidine-2-carboxylate in 75 ml pyridine.After stirring at room temperature for 30 minutes the solution isconcentrated in vacuo and ethyl acetate (300 ml) is added; the solutionis washed twice with 2N hydrochloric acid, once with water and once withsaturated sodium bicarbonate, dried over sodium sulfate, filtered andconcentrated in vacuo. The residue is dissolved in 100 ml ethanol, 5 gof powdered potassium carbonate is added and the mixture stirred 1 hourat room temperature. The solution is filtered, concentrated in vacuo andpurified by flash chromatography using methylene chloride/methanol(95:5) to yield trans ethyl1-acetyl-4-(2-hydroxyethyl)-piperidine-2-carboxylate.

A mixture of 3.7 g of trans ethyl1-acetyl-4-(2-hydroxy-ethyl)-piperidine-2-carboxylate and 5.4 g ofpyridinium chlorochromate in 75 ml methylene chloride is stirred undernitrogen for 2 hours. The mixture is filtered and purified by flashchromatography using ethyl acetate/hexane (7:3 to 8:2) to yield transethyl 1-acetylpiperidine-2-carboxyl-ate-4-acetaldehyde.

EXAMPLE 31

A mixture of 2.5 g of trans ethyl4-[1-(3-diethylphosphono-prop-2-enyl)]-1-acetylpiperidine-2-carboxylateand 40 ml 6N hydrochloric acid is refluxed for 12 hours. The solution isconcentrated in vacuo to dryness. The residue is dissolved in 20 ml ofethanol and 2.3 ml of propylene oxide added. The solid that separates isfiltered off and dried in vacuo to yield trans4-[1-(3-phosphonoprop-2-enyl)]-piperidine-2-carboxylic acid, m.p.132°-140°.

EXAMPLE 32

A solution of 0.334 g of trans ethyl4-[1-(3-bromoprop-1-enyl)]-1-(tert-butoxycarbonyl)-piperidine-2-carboxylateand 3.5 ml of triethylphosphite is refluxed under nitrogen for 70minutes. The cooled solution is concentrated in vacuo and purified byflash chromatography using methylene chloride/methanol (100:3) to yieldtrans ethyl4-[1-(3-diethylphosphonoprop-1-enyl)]-1-(tert-butoxycarbonyl)-piperidine-2-carboxylate.

The starting material is prepared as follows:

A solution of 20 g 4-pyridylcarbinol, 28.9 g ofchlorotert-butyl-dimethylsilane and 14.4 g imidazole in 200 mldimethylformamide is stirred 3 hours at room temperature. Product isisolated by extraction into ethyl acetate/hexane (1:1) and washingextract 4 times with 400 ml of water. The solution is filtered throughsilica gel and concentrated in vacuo to yield4-(tert-butyl-dimethylsilyloxymethyl)pyridine.

A solution of 40.6 g of 4-(tert-butyl-dimethylsilyloxymethyl)-pyridineand 40 g of m-chloroperbenzoic acid in 500 ml methylene chloride isstirred 16 hours at room temperature. Solution is washed with 2N sodiumhydroxide and water, dried over sodium sulfate, filtered andconcentrated in vacuo to yield4-(tert-butyldimethylsilyloxymethyl)-pyridine-N-oxide.

A solution of 37.9 g of4-(tert-butyl-dimethylsilyloxymethyl)-pyridine-N-oxide, 84 ml oftrimethylsilyl cyanide and 44 ml triethylamine is stirred under nitrogenat reflux for 21/2 hours. Dark solution is cooled in an ice bath, then40 ml of ethanol added followed by 500 ml of ethyl acetate. The solutionis washed twice with water, dried over sodium sulfate, filtered,concentrated in vacuo and purified by flash chromatography using ethylacetate/hexane (1:10) to yield4-(tert-butyl-dimethylsilyloxymethyl)-2-cyanopyridine.

A solution of 21.7 g of4-(tert-butyl-dimethylsilyloxymethyl)-2-cyanopyridine in 220 mlanhydrous ethanol containing 0.2 g of sodium is stirred at roomtemperature for 18 hours, cooled to 0° and 22 ml 6N hydrochloric acid isthen added. The solution is stirred at room temperature for 18 hourscooled to 0°, 7.5 ml 6N sodium hydroxide added followed by 20 mlsaturated aqueous sodium carbonate. Extraction with methylene chloride,then drying, filtering and concentrating the extract yields an oil whichcrystallizes from ether to yield ethyl4-(hydroxymethyl)pyridine-2-carboxylate.

A mixture of 13.9 g of ethyl 4-(hydroxymethyl)-pyridine-2-carboxylate, 5g platinum oxide in 250 ml acetic acid is hydrogenated at 50 lbs/in².Filtration, concentration in vacuo, and neutralization with potassiumcarbonate in methylene chloride yields an oil that is purified by flashchromatography using methylene chloride/methanol saturated with ammonia(20:1) to yield ethyl 4-(hydroxymethyl)-piperidine-2-carboxylate.

A solution of 5.16 g of ethyl 4-(hydroxymethyl)-piperidine-2-carboxylateand 6.33 g di-tert-butyl dicarbonate in 100 ml of methylene chloride isstirred at room temperature for 18 hours. The solution is concentratedin vacuo to yield ethyl1-(tert-butoxycarbonyl)-4-(hydroxymethyl)-piperidine-2-carboxylate.

A solution of 7.9 g of ethyl1-(tert-butoxycarbonyl)-4-(hydroxymethyl)-piperidine-2-carboxylate and9.9 g of pyridinium chlorochromate in 175 ml of methylene chloride isstirred at room temperature for 3 hours. The mixture is filtered andpurified by flash chromatography using ethyl acetate/hexane (25:75) toyield1-(tert-butoxycarbonyl)-2-ethoxycarbonylpiperidine-4-carboxaldehyde.

A solution of 1 g of1-(tert-butoxycarbonyl)-2-ethoxycarbonylpiperidine-4-carboxaldehyde and2 g of formylmethylene-triphenylphosphoran in 16 ml of toluene is heatedto 100° (bath) for 2 hours. The solution is cooled and purified by flashchromatography using ethyl acetate/hexane (25:75) to yield1-(tert-butoxycarbonyl)-2-ethoxycarbonylpiperidine-4-acrylaldehyde.

A solution of 0.83 g of1-tert-butoxycarbonyl-2-ethoxycarbonyl-piperidine-4-acrylaldehyde and0.11 g of sodium borohydride in 8 ml of ethanol is stirred at 0° for 30minutes; 0.2 ml of acetic acid is added followed by ice cold water andthe mixture is extracted with methylene chloride. The extract is driedover sodium sulfate, filtered and concentrated in vacuo. Purification byflash chromatography using ethylacetate/hexane (25:75) yields transethyl1-(tert-butoxycarbonyl)-4-[1-(3-hydroxyprop-1-enyl)]-piperidine-2-carboxylate.

A solution of 0.367 g of ethyl1-tert-butoxycarbonyl-4-[1-(3-hydroxyprop-1-enyl)]-piperidine-2-carboxylate,0.35 g triphenylphosphine and 0.23 of bromosuccinimide in 8 ml ofmethylene chloride is stirred initially at 0° and then at roomtemperature for 40 minutes. Purification by flash chromatography usingethyl acetate/hexane (1:9) yields trans ethyl4-[1-(3-bromoprop-1-enyl)]-1-(tert-butoxycarbonyl)piperidine-2-carboxylate

EXAMPLE 33

A solution of 0.39 g of trans ethyl4-[1-(3-diethylphosphono-prop-1-enyl)]-1-(tert-butoxycarbonyl)-piperidine-2-carboxylateand 2.3 ml of trifluoroacetic acid in 8 ml of methylene chloride isstirred at room temperature for 30 minutes. Saturated aqueous sodiumbicarbonate is added and the mixture extracted with methylene chloride.Purification by flash chromatography using methylene chloride/methanolsaturated with ammonia (20:1) yields trans ethyl4-[1-(3-diethylphosphonoprop-1-enyl)]-piperidine-2-carboxylate.

EXAMPLE 34

A solution of 0.265 g of trans ethyl4-[1-(3-diethylphosphonoprop-1-enyl)]-piperidine-2-carboxylate in 5 mlof anhydrous ethanol containing 0.074 ml of butyl lithium (1.6M) isheated at 80° (bath) for 72 hours. After cooling, 0.025 ml acetic acidis added, followed by excess saturated sodium bicarbonate, and themixture is extracted with methylene chloride. The methylene chlorideextract on concentration is vacuo yields an oil; purification by flashchromatography using methylene chloride/isopropanol saturated withammonia (20:1) yields cis ethyl4-[1-(3-diethylphosphonoprop-1-enyl)]-piperidine-2-carboxylate.

EXAMPLE 35

a) A mixture of 0.142 g of cis ethyl4-[1-(3-diethylphosphonoprop-1-enyl]-piperidine-2-carboxylate and 2.5 mlof 6N hydrochloric acid is refluxed for 12 hours. The solution isconcentrated in vacuo to dryness. The residue is dissolved in 2 ml ofethanol and 0.15 ml of propylene oxide is added. The solid thatseparates is filtered off and dried in vacuo to yield cis4-[1-(3-phosphonoprop-1-enyl)]-piperidine-2-carboxylic acid, m.p. 175°dec.; hydrochloride salt, m.p. 130° dec.

b) Similarly, hydrolysis of the trans ester of example 33 yields thecorresponding trans acid, m.p. 130°-135°.

c) A solution of cis4-[1-(3-phosphonoprop-1-enyl)]-piperidine-2-carboxylic acid in saturatedethanolic hydrochloric acid is heated under reflux overnight. Thesolvent is removed in vacuo. A solution of the residue in ethanol istreated with propylene oxide and evaporated to dryness to yield cisethyl 4-[1-(3-phosphonoprop-1-enyl)]piperidine-2-carboxylate.

EXAMPLE 36

To a solution of 0.234 g of trans1-ethoxycarbonyl-2-ethoxycarbonyl-pyrrolidine-3-propionaldehyde in 5 mlof anhydrous tetrahydrofuran under nitrogen, cooled to -78°, is addedslowly a solution of 0.23 ml of tetraethylmethylenediphosphonate and0.57 ml of butyllithium (1.6M) in 5 ml of anhydrous tetrahydrofuran alsoat -78°. Solution is refluxed for 14 hours, cooled and treated with 0.15ml of acetic acid; the reaction mixture is concentrated, diluted withwater and extracted with methylene chloride. The extract is dried oversodium sulfate, filtered and concentrated; purification by flashchromatography using ethyl acetate yields trans ethyl1-ethoxycarbonyl-3-[1-(4-diethylphosphonobut-3-enyl)]-pyrrolidine-2-carboxylate.

The starting material is prepared as follows:

A mixture of 50 g of N-(2-cyanoethyl)glycine in 300 ml of ethanolsaturated with hydrogen chloride gas is stirred 1 hour at roomtemperature then refluxed for 1 hour. After cooling the solid isfiltered off and the filtrate neutralized with sodium bicarbonate,filtered again and concentrated to yield ethylN-(ethoxycarbonylmethyl)-β-alaninate.

To a mixture of 49 g of ethyl N-(ethoxycarbonylmethyl)-β-alaninate and30 ml of water cooled to -10° is added dropwise 27.6 ml of ethylchloroformate followed by a solution of 12.7 g of sodium carbonate in 50ml of water. The mixture is warmed to room temperature then heated at55° for 50 minutes. The mixture is cooled, extracted with toluene, theextract is washed with 2N hydrochloric acid and water. The extract isdried over sodium sulfate, filtered, concentrated and distilled in vacuoto yield ethyl N-(ethoxycarbonylmethyl)-N-(ethoxycarbonyl)-β-alaninate.

A solution of 53.9 g of ethylN-(ethoxycarbonylmethyl)-N-(ethoxycarbonyl)-β-alaninate in 200 ml oftoluene is added dropwise to a stirred solution of potassiumhexamethyldisilazide (429 ml, 0,653M) in 125 ml of toluene undernitrogen and cooled to 0°. After 45 minutes at 0°, 21.6 ml of aceticacid is added followed by a solution of 100 g of sodium phosphate(monobasic) in 1 liter of water. The layers are separated, the organiclayer is washed with pH 7 buffer, dried over sodium sulfate, filtered,concentrated and purified by flash chromatography using ethylacetate/hexane (3:7) to yield ethyl1-ethoxycarbonyl-3-oxo-pyrrolidine-2-carboxylate.

To a stirred suspension of 24 g ofbenzyloxycarbonylmethyl-triphenylphosphonium bromide in 225 ml ofanhydrous tetrahydrofuran under nitrogen and cooled to 0° is added 73 mlof potassium hexamethyldisilazide (0.652M). After 10 minutes a solutionof 11 g of ethyl 1-ethoxycarbonyl-3-oxopyrrolidine-2-carboxylate in 50ml of tetrahydrofuran is added and the mixture refluxed 21/2 hours.After cooling the mixture is filtered and concentrated in vacuo. Theresidue is dissolved in ethyl acetate, washed with water, dried oversodium sulfate, filtered, concentrated and purified by flashchromatography using ethyl acetate/hexane (1:4) to yield an oil; this ishydrogenated in 200 ml of ethanol and 5 g of 10% palladium on carbon toyield, after filtering and concentrating the filtrate,1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-acetic acid.

A solution of 10 g of1-ethoxycarbonyl-2-ethoxycarbonyl-pyrrolidine-3-acetic acid in 50 mltetrahydrofuran is cooled to 0° and 55 ml of borane/tetrahydrofuran (1M)is added dropwise. After stirring 2 hours at 0°, 20 ml of water isadded, the mixture is extracted with ethyl acetate, washed twice withwater and dried over sodium sulfate. The solution is filtered,concentrated and purified by flash chromatography using ethylacetate/hexane (1:1 to 7:3) to yield cis1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-ethanol.

A solution of 6 g of cis1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-ethanol in 75 ml ofmethylene chloride containing 7.3 ml of diisopropylethylamine, to whichis added 5.1 ml of 85% benzyloxymethyl chloride, is stirred 31/2 hoursat room temperature. The solution is washed with water and saturatedaqueous sodium bicarbonate. The solution is then dried over sodiumsulfate, filtered, concentrated and purified by flash chromatographyusing ethyl acetate/hexane (1:4) to yield cis ethyl1-ethoxycarbonyl-3-[2-(benzyloxymethoxy)-ethyl]-pyrrolidine-2-carboxylate.

A solution of 6.2 g of cis ethyl1-ethoxycarbonyl-3-[2-(benzyloxymethoxy)ethyl]-pyrrolidine-2-carboxylatein 75 ml of anhydrous ethanol containing 1 ml of butyllithium (1.6M) isrefluxed under nitrogen for 6 days. After cooling, 1.7 ml of 1Nhydrochloric acid is added, the solution is concentrated in vacuo, coldwater added and mixture extracted with methylene chloride. The extractis dried over sodium sulfate, filtered, concentrated and purified byhigh pressure liquid chromatography using ethyl acetate/hexane (15:85)to yield trans ethyl1-ethoxycarbonyl-3-[2-(benzyloxymethoxy)-ethyl]-pyrrolidine-2-carboxylate.

A mixture of 1.64 g of trans ethyl1-ethoxycarbonyl-3-[2-benzyloxymethoxy)-ethyl]-pyrrolidine-2-carboxylateand 2 g of 10% palladium on carbon in 35 ml of acetic acid ishydrogenated at 45 lbs/in². The mixture is filtered, concentrated invacuo and purified by flash chromatography using ethyl acetate/hexane(6:4 to 7:3) to yield trans1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-ethanol.

A solution of 0.991 g of trans1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-ethanol and 1.24 gpyridinium chlorochromate in 20 ml of methylene chloride is stirredunder nitrogen for 4 hours. Mixture is filtered and purified by flashchromatography using ethyl acetate/hexane (1:1) to yield trans1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-acetaldehyde.

To 0.4 g of trans1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-acetaldehyde in 5 mlanhydrous tetrahydrofuran under nitrogen, cooled to -78°, is addeddropwise a solution of 1.17 g of methoxymethyl-triphenylphosphoniumchloride in 15 ml of anhydrous tetrahydrofuran to which is added 1.55 mlof potassium tert-butoxide/tetrahydrofuran (1.6M). Solution is stirredat room temperature for 4 hours. 2N Hydrochloric acid (11 ml) is addedand the mixture is stirred for 45 minutes. The solution is concentratedand then extracted with methylene chloride. The extract is dried oversodium sulfate, filtered, concentrated, and the residue is purified byflash chromatography using ethyl acetate/hexane (1:5 to 3:7) to yieldtrans 1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-propionaldehyde.

EXAMPLE 37

A mixture of 0.193 g of trans ethyl1-ethoxycarbonyl-3-[1-(4-diethylphosphonobut-3-enyl)]-pyrrolidine-2-carboxylateand 4 ml of concentrated hydrochloric acid is refluxed for 16 hours. Thesolution is cooled and concentrated to dryness in vacuo. The solid thatseparates is filtered off and dried in vacuo to yield trans3-[1-(4-phosphonobut-3-enyl)]-pyrrolidine-2-carboxylic acid, m.p.110°-115° dec.

EXAMPLE 38

To a solution of 0.426 g of cis1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-propionaldehyde in 10 mlof anhydrous tetrahydrofuran under nitrogen, cooled to -78°, is addedslowly a solution of 0.45 ml of tetraethylmethylenediphosphonate and1.06 ml of butyllithium (1.6M) in 10 ml of anhydrous tetrahydrofuranalso at -78°. Solution is refluxed 14 hours, cooled and 0.3 ml aceticacid is added; the reaction mixture is concentrated, water is added andthe mixture is extracted with methylene chloride. The extract is driedover sodium sulfate, filtered, concentrated and purified by flashchromatography using ethyl acetate to yield cis ethyl1-ethoxycarbonyl-3-[1-(4-diethylphosphonobut-3-enyl)]-pyrrolidine-2-carboxylate.

The starting material is prepared as follows:

A solution of 0.908 g of cis1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-ethanol and 1.14 gpyridinium chlorochromate in 20 ml of methylene chloride is stirredunder nitrogen for 4 hours. Mixture is filtered and purified by flashchromatography using ethyl acetate/hexane (1:1) to yield cis1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-acetaldehyde.

To 0.663 g of cis1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-acetaldehyde in 10 mlanhydrous tetrahydrofuran under nitrogen, cooled to -78°, is addeddropwise a solution of 2.21 g of methoxymethyl-triphenylphosphoniumchloride in 20 ml of anhydrous tetrahydrofuran to which is added 2.6 mlof potassium tert-butoxide/tetrahydrofuran (1.6M). Solution is stirredat room temperature for 4 hours; 15 ml of 2N hydrochloric acid is addedand the mixture stirred for 45 minutes. The solution is concentrated andthen extracted with methylene chloride. The extract is dried over sodiumsulfate, filtered and concentrated; purification by flash chromatographyusing ethyl acetate/hexane (1:5 to 3:7) yields cis1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-propionaldehyde.

EXAMPLE 39

A mixture of 0.176 g of cis ethyl1-ethoxycarbonyl-3-[1-(4-diethylphosphonobut-3-enyl)]-pyrrolidine-2-carboxylateand 3.5 ml of concentrated hydrochloric acid is refluxed 18 hours. Thesolution is concentrated in vacuo to dryness, the residue dissolved in1.5 ml of isopropanol/methanol (5:1) and 0.2 ml of propylene oxide isadded. The solid that separates is filtered off and dried in vacuo toyield cis 3-[1-(4-phosphonobut-3-enyl)]-pyrrolidine-2-carboxylic isacid, m.p. 132°-140°.

EXAMPLE 40

A solution of 0.0655 g of trans ethyl1-ethoxycarbonyl-3-[1-(4-bromobut-2-enyl]-pyrrolidine-2-carboxylate in0.75 ml of triethylphosphite is refluxed 20 minutes. The solution isconcentrated in vacuo and the residue purified by flash chromatographyusing methylene chloride/ethanol (30:1) to yield trans ethyl1-ethoxycarbonyl-3-[1-(4-diethylphosphono-but-2-enyl)]-pyrrolidine-2-carboxylate.

The starting material is prepared as follows:

A solution of 0.225 g of trans1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-acetaldehyde and 0.4 g of(formylmethylene)-triphenylphosphoran in 2 ml of methylene chloride isrefluxed 44 hours. The solution is concentrated and the residue ispurified by flash chromatography using ethyl acetate/hexane (2:3) toyield trans ethyl1-ethoxycarbonyl-3-[1-(4-oxobut-2-enyl)]-pyrrolidine-2-carboxylate.

To a stirred solution of 0.102 g of trans ethyl1-ethoxycarbonyl-3-[1(4-oxobut-2-enyl)]-pyrrolidine-2-carboxylate in 2ml of ethanol cooled to 0° is added 0.035 g of sodium borohydride. After30 minutes at 0° and 30 minutes at room temperature 0.05 ml of aceticacid is added, the solution concentrated, water added and mixtureextracted with methylene chloride. The solution is dried over sodiumsulfate, filtered and concentrated in vacuo to yield trans ethyl1-ethoxycarbonyl-3-[1-(4-hydroxybut-2-enyl)]-pyrrolidine-2-carboxylate.

To a stirred solution of 0.0937 g of transethyl-1-ethoxycarbonyl-3-[1-(4-hydroxybut-2-enyl)]-pyrrolidine-2-carboxylateand 0.1 g of triphenylphosphine in 2 ml of methylene chloride at 0° isadded 0.067 g of N-bromosuccinimide. After 30 minutes at roomtemperature the mixture is purified by flash chromatography using ethylacetate/hexane (1:3) to yield trans ethyl1-ethoxycarbonyl-3-[1-(4-bromobut-2-enyl)]-pyrrolidine-2-carboxylate.

EXAMPLE 41

A mixture of 0.053 g of trans ethyl1-ethoxycarbonyl-3-[1-(4-diethylphosphonobut-2-enyl]-pyrrolidine-2-carboxylateand 1.5 ml of concentrated hydrochloric acid is refluxed for 16 hours.The solution is concentrated to dryness in vacuo, the residue isdissolved in 1 ml of methanol, 0.2 ml of propylene oxide is added andthe solution is concentrated. The residue is purified by ion exchangechromatography eluting with 0.1N ammonium hydroxide to yield trans3-[1-(4-phosphonobut-2-enyl)]-pyrrolidine-2-carboxylic acid, m.p.138°-145°.

EXAMPLE 42

Preparation of an injectable formulation containing 10 mg of the activeingredient per 5 ml of solution having a formula as follows:

    ______________________________________                                        cis 4-[1-(3-phosphonoprop-1-enyl)]-                                                                 10.0      g                                             piperidine-2-carboxylic acid                                                  Propylparaben         0.5       g                                             Water for injection q.s.                                                                            5000.0    ml                                            ______________________________________                                    

The active ingredient and preservative are dissolved in 3500 ml of waterfor injection and the solution is diluted to 5000 ml. The solution isfiltered through a sterile filter and filled into injection vials understerile conditions each vial containing 5 ml of the solution.

EXAMPLE 43

a) Preparation of 10,000 tablets each containing 10 mg of the activeingredient, having the formula as follows:

    ______________________________________                                        cis 4-[1-(3-phosphonoprop-1-enyl)]-                                                                100.00      g                                            piperidine-2-carboxylic acid                                                  Lactose              2,535.00    g                                            Corn starch          125.00      g                                            Polyethylene glycol 6,000                                                                          150.00      g                                            Magnesium stearate   40.00       g                                            Purified water       q.s.                                                     ______________________________________                                    

Procedure: All the powders are passed through a screen with openings of0.6 mm. The drug substance, lactose, magnesium stearate and half of thestarch are mixed in a suitable mixer. The other half of the starch issuspended in 65 ml of water and the suspension added to the boilingsolution of the polyethylene glycol in 260 ml of water. The paste formedis added to the powders, which are granulated, if necessary, with anadditional amount of water. The granulate is dried overnight at 35° C.broken on a screen with 1.2 mm openings and compressed into tablets,using concave punches uppers bisected.

Analogously tablets are prepared, containing about 1-50 mg of one of theother compounds disclosed and exemplified herein.

b) Preparation of 1,000 capsules each containing 5 mg of the activeingredient, having the formula as follows:

    ______________________________________                                        cis 4-[1-(3-phosphonoprop-1-enyl)]-                                                                 5.0       g                                             piperidine-2-carboxylic acid                                                  Lactose               212.0     g                                             Modified starch       80.0      g                                             Magnesium stearate    3.0       g                                             ______________________________________                                    

Procedure: All the powders are passed through a screen with openings of0.6 mm. Then the drug substance is placed in a suitable mixer and mixedfirst with the magnesium stearate, then with the lactose and starchuntil homogeneous. No. 2 hard gelatin capsules are filled with 300 mg ofsaid mixture each, using a capsule filing machine.

Analogously capsules are prepared, containing about 1-50 mg of the othercompounds disclosed and exemplified herein.

What is claimed is:
 1. A compound according to claim 1 of the formula##STR12## or a perhydroquinoline derivative thereof, wherein Arepresents lower alkylene, lower alkenylene or a direct bond; R and R'represent hydrogen, lower alkyl, benzyl, benzyl substituted on phenyl byhalogen, lower alkyl or lower alkoxy; or R and R' represent loweralkanoyloxymethyl, lower alkanoyloxymethyl substituted on oxymethyl bylower alkyl, cyclohexyl or cyclopentyl; COR₁ represents carboxy orcarboxy functionalized in the form of a pharmaceutically acceptableproducing ester or carbamoyl; R₂ represents hydrogen, lower alkyl,aryl-lower alkyl, or acyl; R₄ represents hydrogen, lower alkyl, loweralkoxy, halogen or trifluoromethyl; or a pharmaceutically acceptablesalt thereof.
 2. A compound according to claim 1 of the formula##STR13## or a perhydroquinoline derivative thereof wherein n representsthe integer 1, 2 or 3; R and R' independently represent hydrogen, loweralkyl, benzyl, lower alkanoyloxymethyl or lower alkanoyloxymethylsubstituted on oxymethyl by lower alkyl; COR₁ represents carboxy,carboxy esterified in the form of a pharmaceutically acceptableproducing ester, or carbamoyl; R₂ represents hydrogen, lower alkyl,lower alkanoyl, benzoyl or benzoyl substituted by lower alkyl, by loweralkoxy, by halogen or by trifluoromethyl; or a pharmaceuticallyacceptable salt thereof.
 3. A cis compound according to claim
 2. 4. Acompound according to claim 2 wherein n represents the integer 1, 2 or3; R and R' both represent hydrogen or lower alkanoyloxymethyl; or oneof R and R' represents hydrogen and the other of R and R' representslower alkyl, benzyl, lower alkanoyloxymethyl, or lower alkanoyloxymethylsubstituted on oxymethyl by lower alkyl; R₂ represents hydrogen; COR₁represents carboxy or carboxy esterified in form of a pharmaceuticallyacceptable producing ester.
 5. A compound according to claim 2 offormula V or a perhydroquinoline derivative thereof wherein n representsthe integer 1; R and R' represent hydrogen; COR₁ represents carboxy orcarboxy esterified in form of a pharmaceutically acceptable producingester; R₂ represents hydrogen; or a pharmaceutically acceptable saltthereof.
 6. A compound according to claim 1 of formula IV or aperhydroquinoline derivative thereof wherein A is attached at the 4position and represents 1,3-propenylene with double bond adjacent to thephosphono grouping; R, R' and R₂ and R₄ represent hydrogen; COR₁represents carboxy or carboxy esterified in form of a pharmaceuticallyacceptable producing ester; or a pharmaceutically acceptable saltthereof.
 7. A compound according to claim 2 which iscis-4-(3-phosphonopropyl)-1,2,3,4-tetrahydroquinoline-2-carboxylic acidor a pharmaceutically acceptable salt thereof.
 8. A compound accordingto claim 2 which is cis-4-phosphonomethylperhydroquinoline-2-carboxylicacid or a pharmaceutically acceptable salt thereof.
 9. A pharmaceuticalcomposition suitable for the blockade of the N-methyl-D-aspartateexcitatory amino acid receptor in a mammal comprising a correspondinglyeffective amount of a compound of claim 1 in combination with one ormore pharmaceutically acceptable carriers.
 10. A method of blocking theN-methyl-D-aspartate excitatory amino acid receptor in a mammalcomprising the administration to a mammal in need thereof of acorrespondingly effective amount of a compound of claim 1 or of apharmaceutical composition comprising said compound.
 11. A method oftreating diseases responsive to N-methyl-D-aspartate excitatory aminoacid receptor blockade in mammals comprising the administration to amammal in need thereof of an effective N-methyl-D-aspartate excitatoryamino acid receptor blocking amount of a compound of claim 1 or of apharmaceutical composition comprising said compound.
 12. A method oftreating cerebral ischemia and of inhibiting brain damage resulting fromcerebral ischemia in mammals which comprises the administration to amammal in need thereof of an effective amount of a compound of claim 4or of a pharmaceutical composition comprising said compound.